Chapter 4—Medical devices
Part 4‑1—Introduction
Division 1—Overview of this Chapter
41B General
The purpose of this Chapter is to ensure the safety and satisfactory performance of medical devices. It does this by:
(a) setting out particular requirements for medical devices; and
(b) establishing administrative processes principally aimed at ensuring those requirements are met; and
(c) providing for enforcement through a series of offences and civil penalty provisions.
41BA Requirements for medical devices (Parts 4‑2 and 4‑3)
The requirements for medical devices are:
(a) essential principles (that are about the safety and performance characteristics of medical devices); and
(b) conformity assessment procedures (that are mainly about the application of quality management systems) or requirements comparable to conformity assessment procedures.
Note: Medical device standards may be made under Division 2 of Part 4‑2, and conformity assessment standards may be made under Division 2 of Part 4‑3, but they are not requirements.
41BB Administrative processes (Parts 4‑4 to 4‑10)
The administrative processes under this Chapter are:
(a) issuing conformity assessment certificates for some manufacturers of medical devices; and
(aa) making conformity assessment body determinations; and
(b) including medical devices in the Register; and
(c) suspending or cancelling entries of medical devices from the Register; and
(ca) exempting medical devices from various provisions of this Chapter to deal with emergency situations; and
(d) exempting medical devices from the requirement to be included in the Register; and
(e) obtaining information about medical devices; and
(f) requiring public notification of problems with medical devices, and recall of such devices.
Note: Part 4‑10 provides for assessment fees to be payable in some circumstances.
41BC Enforcement (Part 4‑11)
Part 4‑11 contains offences and civil penalty provisions that are aimed at ensuring that:
(a) the requirements for medical devices are complied with; and
(b) the administrative processes under this Chapter (particularly the inclusion of medical devices in the Register) are followed.
Note: There are some offences and civil penalty provisions in Parts 4‑4 to 4‑9. They generally relate to matters ancillary to administrative processes in those Parts (e.g. false or misleading statements in applications).
Division 2—Interpretation
41BD What is a medical device
(1) A medical device is:
(a) any instrument, apparatus, appliance, software, implant, reagent, material or other article (whether used alone or in combination, and including the software necessary for its proper application) intended, by the person under whose name it is or is to be supplied, to be used for human beings for the purpose of one or more of the following:
(i) diagnosis, prevention, monitoring, prediction, prognosis, treatment or alleviation of disease;
(ii) diagnosis, monitoring, treatment, alleviation of or compensation for an injury or disability;
(iii) investigation, replacement or modification of the anatomy or of a physiological or pathological process or state;
(iv) control or support of conception;
(v) in vitro examination of a specimen derived from the human body for a specific medical purpose;
and that does not achieve its principal intended action in or on the human body by pharmacological, immunological or metabolic means, but that may be assisted in its function by such means; or
(aa) any instrument, apparatus, appliance, software, implant, reagent, material or other article specified under subsection (2A); or
(ab) any instrument, apparatus, appliance, software, implant, reagent, material or other article that is included in a class of instruments, apparatus, appliances, software, implants, reagents, materials or other articles specified under subsection (2B); or
(b) an accessory to an instrument, apparatus, appliance, software, implant, reagent, material or other article covered by paragraph (a), (aa) or (ab); or
(c) a system or procedure pack.
Note: Declarations under subsection (3) exclude articles from the scope of this definition. Declarations under section 7 can also have this effect: see subsection 7(4).
(2) For the purposes of paragraph (1)(a), the purpose for which an instrument, apparatus, appliance, software, implant, reagent, material or other article (the main equipment) is to be used is to be ascertained from the information supplied, by the person under whose name the main equipment is or is to be supplied, on or in any one or more of the following:
(a) the labelling on the main equipment;
(b) the instructions for using the main equipment;
(c) any advertising material relating to the main equipment;
(d) technical documentation describing the mechanism of action of the main equipment.
(2A) The Secretary may, by notice published in the Gazette or on the Department’s website, specify a particular instrument, apparatus, appliance, software, implant, reagent, material or other article for the purposes of paragraph (1)(aa). The notice is not a legislative instrument.
(2B) The Secretary may, by legislative instrument, specify a particular class of instruments, apparatus, appliances, software, implants, reagents, materials or other articles for the purposes of paragraph (1)(ab).
(3) The Secretary may, by order published in the Gazette or on the Department’s website, declare that a particular instrument, apparatus, appliance, software, implant, reagent, material or other article, or that a particular class of instruments, apparatus, appliances, software, implants, reagents, materials or other articles, are not, for the purposes of this Act, medical devices.
Note: A declaration under this section does not stop articles from being therapeutic goods.
(4) A declaration under this section takes effect on the day on which the declaration is published in the Gazette or on the Department’s website or on such later day as is specified in the order.
41BE Kinds of medical devices
General
(1) For the purposes of this Chapter, a medical device is taken to be of the same kind as another medical device if they:
(a) have the same sponsor; and
(b) have the same manufacturer; and
(c) have the same device nomenclature system code (see subsection (3)); and
(d) have the same medical device classification; and
(e) are the same in relation to such other characteristics as the regulations prescribe, either generally or in relation to medical devices of the kind in question.
Unique medical devices
(2) If a medical device is not of the same kind as any other medical device:
(a) this Chapter applies in relation to the device as if it were a kind of medical device; and
(b) references in this Chapter to delivering a reasonable number of samples of the kind of device are taken to be references to delivering the device.
Device nomenclature codes
(3) The Minister may, by legislative instrument, determine device nomenclature codes for medical devices.
41BEA Excluded purposes
The Secretary may, by legislative instrument, specify purposes for the purposes of paragraph 41FD(ia) and subsection 41FF(1A).
41BF System or procedure packs
Two or more goods (including at least one medical device) are a system or procedure pack if:
(a) all of the goods are to be interconnected or combined for use in a medical or surgical procedure; or
(b) all of the goods are packaged together for use in a medical or surgical procedure.
41BG Manufacturers of medical devices
(1) The manufacturer of a medical device is the person who is responsible for the design, production, packaging and labelling of the device before it is supplied under the person’s name, whether or not it is the person, or another person acting on the person’s behalf, who carries out those operations.
(2) If subsection (1) does not apply to a medical device, the manufacturer of the device is the person who, with a view to supplying the device under the person’s name, does one or more of the following using ready‑made products:
(a) assembles the device;
(b) packages the device;
(c) processes the device;
(d) fully refurbishes the device;
(e) labels the device;
(f) assigns to the device its purpose by means of information supplied, by the person, on or in any one or more of the following:
(i) the labelling on the device;
(ii) the instructions for using the device;
(iii) any advertising material relating to the device;
(iv) technical documentation describing the mechanism of action of the device.
(3) However, a person is not the manufacturer of a medical device if:
(a) the person assembles or adapts the device for an individual patient; and
(b) the device has already been supplied by another person; and
(c) the assembly or adaptation does not change the purpose intended for the device by means of information supplied by that other person, on or in any one or more of the following:
(i) the labelling on the device;
(ii) the instructions for using the device;
(iii) any advertising material relating to the device;
(iv) technical documentation describing the mechanism of action of the device.
(4) A person is not the manufacturer of a medical device if the person is included in a class of persons prescribed by the regulations for the purposes of this subsection.
41BH Meaning of compliance with essential principles
(1) A medical device complies, for the purposes of this Chapter (including Part 4‑11), with the essential principles if and only if it does not contravene any of the essential principles.
(2) However, a medical device is also taken, for the purposes of this Chapter (other than Part 4‑11), to comply with the essential principles if:
(a) the medical device complies with one or more medical device standards that apply to it; and
(b) the medical device contravenes the essential principles only in respect of a part or parts of the essential principles to which that medical device standard, or one or more of those medical device standards, relate.
(3) For the purposes of this section, a medical device standard relates to a part or parts of the essential principles only if the standard specifies that part or parts.
41BI Meaning of non‑application of conformity assessment procedures
(1) A conformity assessment procedure is taken, for the purposes of this Chapter, not to have been applied to a medical device if:
(a) there has been a contravention of the conformity assessment procedures; and
(b) the contravention relates, wholly or partly, to that device or its manufacture.
(2) However, for the purposes of this Chapter (other than Part 4‑11), subsection (1) does not apply if:
(a) the quality management system applied in the manufacture of the medical device complies with one or more conformity assessment standards that apply to it; and
(b) the contravention is only in respect of a part or parts of the conformity assessment procedures to which that conformity assessment standard, or one or more of those conformity assessment standards, relate.
(3) For the purposes of this section, a conformity assessment standard relates to a part or parts of the conformity assessment procedures only if the standard specifies that part or parts.
41BIA Meaning of non‑application of overseas requirements comparable to conformity assessment procedures
(1) A requirement that is comparable to a conformity assessment procedure is taken, for the purposes of this Chapter, not to have been applied to a medical device by the manufacturer of the device if:
(a) there has been a contravention of the requirement; and
(b) the contravention relates, wholly or partly, to that device or its manufacture.
(2) However, for the purposes of this Chapter (other than Part 4‑11), subsection (1) does not apply if:
(a) the quality management system applied in the manufacture of the medical device complies with one or more conformity assessment standards that apply to it; and
(b) the contravention is only in respect of a part or parts of the requirement to which that conformity assessment standard, or one or more of those conformity assessment standards, relate.
41BIB Overseas regulators
(1) An overseas regulator is a body determined in an instrument under subsection (2).
(2) The Secretary may, by notifiable instrument, determine a body for the purposes of subsection (1). The Secretary must be satisfied that the body:
(a) is established outside Australia; and
(b) is empowered to issue certificates or other documents to the effect that the body is satisfied that requirements, comparable to the conformity assessment procedures, have been applied to medical devices by the manufacturers of the devices.
(3) Without limiting subsection (2), the Secretary may determine a body by reference to a designation, recognition, approval or authorisation (however described) of the body:
(a) by one or more countries; or
(b) by another body.
Note: For specification by class, see subsection 13(3) of the Legislation Act 2003.
Division 3—Application provisions
41BJA Application of this Chapter to a biological
(1) Subject to this section, this Chapter does not apply to a biological on and after the commencement of this section.
Biologicals currently included in the Register
(2) If, immediately before the commencement of this section, therapeutic goods that are a biological were included in the Register under this Chapter, this Chapter continues to apply to the biological on and after that commencement until the time the biological is included in the Register under Part 3‑2A.
Note: Section 32DN deals with including the biological under Part 3‑2A.
Pending applications
(3) If:
(a) before the commencement of this section, an application was made under this Chapter for the inclusion in the Register of therapeutic goods that are a biological; and
(b) immediately before that commencement, the application was not finally determined; and
(c) the application had not been withdrawn before that commencement;
this Chapter continues to apply to the biological on and after that commencement until the earliest of the following:
(d) the time the biological is included in the Register under Part 3‑2A;
(e) if the application is unsuccessful when it is finally determined—the time the application is finally determined;
(f) the time the application is withdrawn;
(g) the time the application lapses.
Note: Section 32DN deals with including the biological under Part 3‑2A.
(4) For the purposes of this section, an application is finally determined when the application, and any applications for review or appeals arising out of it, have been finally determined or otherwise disposed of.
Transitional
(5) This Chapter applies to a biological on and after the commencement of this section in relation to things done, or omitted to be done, in relation to the biological before the commencement of this section.
(6) If this Chapter continues to apply to a biological during a period described in subsection (2) or (3), then this Chapter also applies to the biological after the end of that period in relation to things done, or omitted to be done, in relation to the biological during that period.
41BK Application of the Criminal Code
Chapter 2 of the Criminal Code applies to all offences against this Chapter.
Note: Chapter 2 of the Criminal Code sets out the general principles of criminal responsibility.
Part 4‑2—Essential principles and medical device standards
41C What this Part is about
The essential principles set out the requirements relating to the safety and performance characteristics of medical devices. Compliance with applicable medical device standards is not required, but it is one way to establish compliance with essential principles.
Note: Dealing in medical devices that do not comply with the essential principles may be an offence or may contravene a civil penalty provision: see Division 1 of Part 4‑11.
Division 1—Essential principles
41CA Essential principles
(1) The regulations may set out requirements for medical devices.
(2) These requirements are to be known as the essential principles.
Division 2—Medical device standards
41CB Medical device standards
(1) The Minister may, by legislative instrument, make an order determining that:
(a) matters specified in the order constitute a medical device standard for kinds of medical devices identified in the order; and
(b) medical devices of those kinds that comply with the standard are to be treated as complying with those parts of the essential principles specified in the standard.
Note: Section 12 of the Legislation Act 2003 deals with when a legislative instrument commences.
(2) The Minister may, by legislative instrument, vary or revoke an order made under subsection (1).
(3) Despite subsection 14(2) of the Legislation Act 2003, an order under subsection (1) of this section, or a variation of such an order, may make provision in relation to a matter by applying, adopting or incorporating, with or without modification, any matter contained in an instrument or other writing as in force or existing from time to time.
41CC Content of medical device standards
(1) Without limiting the scope of section 41CB, an order establishing a medical device standard for kinds of medical devices may be specified by reference to:
(a) the safety or performance characteristics of the devices; or
(b) a monograph in the British Pharmacopoeia, the European Pharmacopoeia or the United States Pharmacopeia‑National Formulary; or
(c) a monograph in a publication approved by the Minister for the purposes of this subsection; or
(d) such a monograph as modified in a manner specified in the order; or
(e) a standard published by a standards organisation; or
(f) such other matters as the Minister thinks fit.
(2) For the purposes of paragraph (1)(e), these are standards organisations:
(a) Standards Australia;
(b) the International Organisation for Standardization;
(c) the International Electrotechnical Commission;
(d) the European Committee for Standardization;
(e) the European Committee for Electrotechnical Standardization;
(f) any other organisation declared by the Minister by notice published in the Gazette or on the Department’s website.
41CD Inconsistencies between medical device standards
(1) A medical device standard that:
(a) applies to a kind of medical device; and
(b) is inconsistent with another medical device standard that applies only to some of the devices of that kind;
is, to the extent of the inconsistency, of no effect in relation to the devices referred to in paragraph (b).
(2) A medical device standard that applies to a kind of medical device that consists of a combination of component parts takes precedence over any medical device standard that applies to the component parts.
Part 4‑3—Conformity assessment procedures
41D What this Part is about
The conformity assessment procedures set out the requirements relating to the application of quality management systems for medical devices, and other requirements imposed on manufacturers.
Compliance with applicable conformity assessment standards is not required, but it is one way to establish that one or more parts of the conformity assessment procedures have been applied to medical devices.
Note 1: Dealing in medical devices that have not had the conformity assessment procedures applied may be an offence or may contravene a civil penalty provision: see Division 2 of Part 4‑11.
Note 2: See section 41BI on applying the conformity assessment procedures.
Division 1—Conformity assessment procedures
41DA Conformity assessment procedures
(1) The regulations may set out requirements relating to the obligations of manufacturers of medical devices.
(2) These requirements are to be known as the conformity assessment procedures.
(3) The conformity assessment procedures, or any part of the conformity assessment procedures, may:
(a) be limited in their application to one or more medical device classifications; or
(b) apply differently to different medical device classifications, different kinds of medical devices or different manufacturers.
(4) Without limiting subsection (1), the regulations may relate to all or any of the following:
(a) application of quality management systems for the manufacture of medical devices;
(b) certification of compliance with the essential principles, or the quality management systems for the manufacture of medical devices;
(c) notification of, and assessment of, changes to a manufacturer’s product range, product design or quality management systems;
(d) declarations to be made by manufacturers of medical devices that conformity assessment procedures have been applied to the devices;
(e) marks to be affixed to medical devices indicating the application of the conformity assessment procedures to the devices;
(f) monitoring and inspecting the design of medical devices or the manufacturing processes for medical devices;
(g) monitoring the performance of medical devices;
(h) corrective action required in relation to the design, manufacture, packaging, labelling and supply of medical devices;
(i) keeping records of the manufacture of medical devices, the design of medical devices or the manufacturing processes for medical devices.
41DB Medical device classifications
The regulations may specify:
(a) classifications, to be known as medical device classifications, applying to medical devices or kinds of medical devices; and
(b) matters in relation to the classification of medical devices or kinds of medical devices.
Division 2—Conformity assessment standards
41DC Conformity assessment standards
(1) The Minister may, by legislative instrument, make an order determining that:
(a) matters specified in the order constitute a conformity assessment standard for quality management systems identified in the order; and
(b) a quality management system that complies with the standard is to be treated as having had applied to it those parts of the conformity assessment procedures specified in the standard.
Note: Section 12 of the Legislation Act 2003 deals with when a legislative instrument commences.
(2) A conformity assessment standard may be limited to particular kinds of medical devices.
(3) The Minister may, by legislative instrument, vary or revoke an order made under subsection (1).
(4) Despite subsection 14(2) of the Legislation Act 2003, an order under subsection (1) of this section, or a variation of such an order, may make provision in relation to a matter by applying, adopting or incorporating, with or without modification, any matter contained in an instrument or other writing as in force or existing from time to time.
41DD Content of conformity assessment standards
(1) Without limiting the scope of section 41DC, an order establishing a conformity assessment standard for a kind of medical device may be specified by reference to:
(a) procedures to be carried out under the quality management systems for the design, manufacture and final inspection of the devices; or
(b) a standard published by a standards organisation; or
(c) such other matters as the Minister thinks fit.
(2) For the purposes of paragraph (1)(b), these are standards organisations:
(a) Standards Australia;
(b) the International Organisation for Standardization;
(c) the European Committee for Standardization;
(d) any other organisation declared by the Minister by notice published in the Gazette or on the Department’s website.
41DE Inconsistencies between conformity assessment standards
A conformity assessment standard that:
(a) identifies quality management systems to which it applies; and
(b) is inconsistent with another conformity assessment standard that applies only to particular kinds of medical devices;
is, to the extent of the inconsistency, of no effect in relation to the devices referred to in paragraph (b).
Part 4‑4—Conformity assessment certificates
41E What this Part is about
The Secretary can issue a conformity assessment certificate (which may be limited to some medical devices) in respect of a manufacturer of medical devices, signifying one or more of these:
(a) that relevant quality management systems have been applied to the device;
(b) the essential principles for the device have been complied with;
(c) other certification requirements of the conformity assessment procedures have been met.
Note: A conformity assessment certificate may be required for an application to include a kind of medical device in the Register to pass preliminary assessment: see paragraph 41FDB(2)(e).
Division 1—Issuing conformity assessment certificates
41EA When conformity assessment certificates are required
The regulations may prescribe:
(a) kinds of manufacturers in respect of whom a conformity assessment certificate must be issued before valid applications can be made for kinds of medical devices, manufactured by those manufacturers, to be included in the Register; or
(b) kinds of medical devices in respect of which a conformity assessment certificate must be issued before valid applications can be made for those kinds of medical devices to be included in the Register.
Note: The regulations may prescribe different levels of fees for different kinds of manufacturers and medical devices: see subsection 41LA(2).
41EB Applications
(1) An application for a conformity assessment certificate must:
(a) be made in accordance with a form approved, in writing, by the Secretary or in such other manner as is approved, in writing, by the Secretary; and
(b) be delivered to an office of the Department specified by the Secretary.
Note: A conformity assessment fee is payable under section 41LA for consideration of the application.
(2) An application is not effective if:
(a) the prescribed application fee has not been paid; or
(b) the application contains information that is false or misleading in a material particular.
Note: A person might also commit an offence, or contravene a civil penalty provision, if the person makes a statement in an application that is false or misleading in a material particular: see sections 41EI and 41EIA.
(3) An approval of a form may require or permit an application or information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
(4) The Secretary may, by written notice given to an applicant for a conformity assessment certificate, require the applicant to allow an authorised person, at any reasonable time specified in the notice, to inspect:
(a) the premises (including premises outside Australia) and equipment, processes and facilities that are being or will be used to manufacture medical devices of the kind in question; and
(b) any other kinds of medical devices on those premises.
41EC Considering applications
(1) If the application is made in accordance with section 41EB, the Secretary must decide whether to issue the conformity assessment certificate.
(2) In deciding whether to issue the certificate, the Secretary must consider some or all aspects of whether the conformity assessment procedures relating to one or more of the following have been applied to the medical device:
(a) the application of quality management systems for the manufacture of medical devices;
(b) the certification of compliance with the essential principles;
(c) any other requirement of the conformity assessment procedures specified in regulations made for the purposes of this subsection.
(3) In deciding whether to issue the certificate, the Secretary must also consider:
(a) whether at least one of the following persons:
(i) the applicant;
(ii) a person (a manager) who makes, or participates in making, decisions that affect the whole, or a substantial part, of the applicant’s affairs;
(iii) if the applicant is a body corporate—a major interest holder of the body corporate;
has, within the 10 years immediately before the application:
(iv) been convicted of an offence against this Act or a corresponding State law; or
(v) been convicted of an offence against a law of the Commonwealth or a law of a State or Territory involving fraud or dishonesty; or
(vi) been ordered to pay a pecuniary penalty for the contravention of a civil penalty provision of this Act or a corresponding State law; or
(vii) been ordered to pay a pecuniary penalty for the contravention of a civil penalty provision of a law of the Commonwealth or a law of a State or Territory involving fraud or dishonesty; or
(viii) breached a condition of a conformity assessment document; or
(ix) had a conformity assessment document suspended or revoked; or
(x) been a manager, or a major interest holder, of a body corporate in respect of which subparagraph (iv), (v), (vi), (vii), (viii) or (ix) applies in that 10 year period, if the conduct resulting in that subparagraph applying occurred when the person was a manager or major interest holder of the body corporate; or
(b) whether any other circumstances prescribed by the regulations for the purposes of this paragraph exist.
(4) A reference in paragraph (3)(a) to a person convicted of an offence includes a reference to a person in respect of whom an order has been made relating to the offence under:
(a) section 19B of the Crimes Act 1914; or
(b) a corresponding provision of a law of a State or Territory.
Note: Section 19B of the Crimes Act 1914 empowers a court that has found a person to have committed an offence to take action without proceeding to record a conviction.
(5) Paragraph (3)(a) does not limit paragraph (3)(b).
(6) The Secretary may, by written notice given to the applicant, require the applicant:
(a) to deliver to the office to which the application was made a reasonable number of samples of the kind of medical device to which the application relates within the period, of not less than 14 days after the day the notice is given, specified in the notice; and
(b) to do so in a manner specified in the notice.
41ECA Conformity assessment (priority applicant) determinations
(1) The regulations may make provision for and in relation to empowering the Secretary to make conformity assessment (priority applicant) determinations.
(2) A conformity assessment (priority applicant) determination is a determination that, for the purposes of this Act, a specified person is a priority applicant in relation to any section 41EB application that may be made by the person for a conformity assessment certificate in relation to medical devices of a kind specified in the determination.
(3) The regulations may make provision for and in relation to the following matters:
(a) applications for conformity assessment (priority applicant) determinations;
(b) the approval by the Secretary of a form for such an application;
(c) information that must accompany such an application;
(d) the application fee for such an application;
(e) empowering the Secretary to give the applicant a written notice requiring the applicant to give to the Secretary specified information or documents in connection with the application within a specified period (which must be at least 10 working days after the notice is given to the applicant).
(4) The regulations may make provision for and in relation to the following matters:
(a) empowering the Secretary to revoke a conformity assessment (priority applicant) determination;
(b) the consequences of the revocation of a conformity assessment (priority applicant) determination.
(5) Subsections (3) and (4) do not limit subsection (1).
(6) The regulations may make provision for and in relation to the priority to be given by the Secretary to consideration of a section 41EB application where the applicant is a priority applicant.
(7) The regulations may provide that, if:
(a) a person is a priority applicant in relation to a section 41EB application made by the person; and
(b) a decision is made on the application;
a statement setting out the decision may be published on the Department’s website.
(8) The express references in this section to the Secretary do not, by implication, prevent the regulations from empowering the Secretary to delegate any or all of the Secretary’s functions or powers under regulations made for the purposes of this section.
(9) If a conformity assessment (priority applicant) determination is in force under the regulations, the determination may be published on the Department’s website.
(10) A conformity assessment (priority applicant) determination made under the regulations is not a legislative instrument.
(11) Subsection 33(3AB) of the Acts Interpretation Act 1901 does not apply to the specification of a person in a conformity assessment (priority applicant) determination.
Note: Subsection 33(3AB) of the Acts Interpretation Act 1901 deals with specification by class.
41ED Time for making decisions on applications
If the application relates to the issuing of a conformity assessment certificate in relation to which a period has been prescribed under paragraph 63(2)(dc), a decision on the application must be made within that period, unless the application lapses under section 41EG.
41EE Procedure following making a decision whether to issue certificate
(1) After making a decision whether to issue a conformity assessment certificate, the Secretary must:
(a) notify the applicant in writing of his or her decision within 20 working days; and
(b) if the decision is not to issue the certificate—state in the notice the reasons for the decision; and
(c) if the decision is to issue the certificate and all assessment fees that are due and payable for the application have been paid:
(i) issue the certificate to the manufacturer in relation to whom the application was made; and
(ii) give the applicant a copy of the certificate (if the applicant is not the manufacturer).
(2) A conformity assessment certificate must specify whether it covers:
(a) all medical devices manufactured by the manufacturer; or
(b) only specified medical devices manufactured by the manufacturer.
(3) A conformity assessment certificate must contain any other information prescribed by the regulations for the purposes of this subsection.
41EF Duration of certificate
(1) The conformity assessment certificate commences on the day specified for the purpose in the certificate. The certificate must specify the period for which it is to be in force (which must be no longer than 5 years).
(2) A conformity assessment certificate has effect at all times:
(a) unless the certificate is suspended under Division 3; or
(b) until the end of the period specified in the certificate, or if the Secretary extends that period, until the end of that extended period; or
(c) until the certificate is revoked under Division 4.
Extensions
(3) The Secretary may, in writing and on his or her own initiative, extend the period for which a conformity assessment certificate is in force.
(4) An extension must be no longer than 12 months.
(5) Only one extension may be given.
(6) The Secretary:
(a) must give notice of an extension to the manufacturer in relation to whom the certificate was issued; and
(b) may give notice of an extension to the applicant for the certificate (if the applicant is not the manufacturer).
41EG Lapsing of applications
An application for a conformity assessment certificate lapses if:
(a) the applicant does not deliver to the office to which the application was made such information (in a form approved in writing by the Secretary) as will allow the certificate to be issued; or
(b) the applicant does not comply with a requirement by the Secretary under subsection 41EC(6) to deliver to the office to which the application was made a reasonable number of samples of the kind of medical device to which the application relates; or
(c) the applicant fails to comply with a notice under section 41JA to give to the Secretary information within a further 10 working days from the day specified in the notice; or
(d) information given to the Secretary by, or on behalf of, the applicant in connection with the application, including information given for the purpose of a notice under section 41JA, is false or misleading in a material particular; or
(e) the applicant fails to allow an authorised person to carry out any inspection as required under subsection 41EB(4); or
(f) for the whole or a part of the conformity assessment fee for the application that is due and payable in accordance with regulations made for the purposes of Part 4‑10—the applicant fails to pay that whole or part in accordance with those regulations.
41EH Treating applications as having been refused
(1) The applicant for an application for a conformity assessment certificate may give the Secretary written notice that the applicant wishes to treat the application as having been refused if:
(a) a period is prescribed under paragraph 63(2)(dc) for making a decision on the application; and
(b) at the end of the period, the applicant has not been notified of a decision whether to issue the certificate.
(2) The notice may be given at any time before the applicant is notified of the decision.
(3) If a notice has been given, this Act (except for subsection 60(5)) has effect as if:
(a) the Secretary had decided not to issue the certificate; and
(b) the Minister had made a decision under subsection 60(3) confirming the decision of the Secretary; and
(c) the Minister’s decision had been made on the day on which notice was given to the Secretary.
41EI Criminal offences for making a false statement
(1) A person commits an offence if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the statement is made in or in connection with an application for a conformity assessment certificate; and
(c) the person knows that the statement is false or misleading in a material particular; and
(d) either:
(i) the use of the kind of medical device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the kind of medical device, if the kind of medical device were used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the statement is in or in connection with an application for a conformity assessment certificate; and
(c) the person knows that the statement is false or misleading in a material particular.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(5) A person commits an offence if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the statement is in or in connection with an application for a conformity assessment certificate; and
(c) the statement is false or misleading in a material particular.
Penalty: 100 penalty units.
(6) An offence against subsection (5) is an offence of strict liability.
41EIA Civil penalty for making a false statement
A person contravenes this section if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the statement is false or misleading in a material particular; and
(c) the statement is in or in connection with an application for a conformity assessment certificate.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Division 2—Conditions
Note: Breaching conditions of the conformity assessment certificate may lead to suspension or revocation of the certificate (see Divisions 3 and 4), may be an offence (see subsections 41MN(5), (8) and (8A)), and may contravene a civil penalty provision (see subsection 41MNA(2)).
41EJ Automatic conditions on conformity assessment certificates
Entry and inspection powers
(1) A conformity assessment certificate is subject to the conditions that the manufacturer in respect of whom the certificate is issued will:
(a) allow an authorised person:
(i) to enter, at any reasonable time, premises (including premises outside Australia) at which the person or any other person deals with medical devices of a kind covered by the certificate; and
(ii) while on those premises, to inspect those premises and medical devices of any kind on those premises and to examine, take measurements of, conduct tests on, require tests to be conducted on or take samples of medical devices of any kind on those premises or any thing on those premises that relates to medical devices of any kind; and
(iii) while on those premises, to make any still or moving image or any recording of those premises or any thing on those premises; and
(b) if requested to do so by an authorised person:
(i) produce to the person such documents relating to devices of a kind covered by the certificate, or to the manufacturer’s quality management system, as the person requires; and
(ii) allow the person to copy the documents.
Review
(2) A conformity assessment certificate is subject to the condition that the manufacturer in respect of whom the certificate is issued will cooperate in any review by the Secretary of the certificate to determine whether the conformity assessment procedures relating to the following matters have been applied to the kinds of medical devices covered by the certificate:
(a) the application of quality management systems for the manufacture of medical devices;
(b) the certification of compliance with the essential principles;
(c) any other requirement of the conformity assessment procedures specified in the regulations made for the purposes of subsection 41EC(2).
Notification of substantial changes
(3) A conformity assessment certificate is subject to the condition that the person in respect of whom the certificate is issued will notify the Secretary, in writing, of any plan for substantial changes to:
(a) quality management systems; or
(b) the product range covered by those systems; or
(c) the product design of kinds of medical devices;
in respect of which the certificate is issued.
Fees
(4) A conformity assessment certificate is subject to the condition that the applicant for the certificate will pay a fee, prescribed in the regulations, for a review under subsection (2), when the fee becomes due and payable.
(5) The regulations may prescribe different levels of fees for different kinds of manufacturers and medical devices.
Conditions in regulations
(5A) A conformity assessment certificate is subject to any conditions prescribed by the regulations for the purposes of this subsection.
Conditions do not limit other conditions
(6) A condition imposed under this section is in addition to any conditions imposed under this Division.
41EK Conditions imposed when conformity assessment certificates are issued
If the Secretary issues a conformity assessment certificate in respect of a manufacturer, the Secretary may, in writing, impose conditions on the certificate in respect of:
(a) one or more kinds of medical devices covered by the certificate; or
(b) the manufacturer’s quality management system.
41EL Conditions imposed after issuing a conformity assessment certificate
(1) The Secretary may, by written notice given to a manufacturer in respect of whom a conformity assessment certificate has been issued:
(a) impose new conditions on the certificate in respect of:
(i) one or more kinds of medical devices covered by the certificate; or
(ii) the manufacturer’s quality management system; or
(b) vary or remove existing conditions.
The power may be exercised at the request of the applicant for the certificate or on the Secretary’s own initiative.
(2) The imposition, variation or removal of a condition under this section takes effect:
(a) if the notice states that the action is necessary to prevent imminent risk of death, serious illness or serious injury—on the day on which the notice is given to the person; or
(aa) in the case of an imposition or variation requested by the person, and to which paragraph (a) does not apply—on the day specified in the notice, which must be at least 20 working days after the notice is given to the person, unless the person has agreed to an earlier day; or
(ab) in the case of a removal to which paragraph (a) does not apply—on the day specified in the notice, which must be at least 20 working days after the notice is given to the person, unless the person has agreed to an earlier day; or
(b) in any other case—on the day specified for the purpose in the notice, being a day not earlier than 20 working days after the notice is given to the person.
(3) For the purposes of paragraphs (2)(aa) and (ab), the earlier day must not be earlier than the day the notice is given to the person.
Division 3—Suspension of conformity assessment certificates
41EM Suspension of conformity assessment certificates
(1) The Secretary may, by written notice given to the person in relation to whom a conformity assessment certificate is issued, suspend the certificate if the Secretary is satisfied that it is likely that there are grounds for revoking the certificate under section 41ET.
(2) The suspension may be limited to some medical devices of that kind, as specified in the notice.
(3) The notice must specify the period of the suspension. The period must not exceed 6 months.
Note: The period of the suspension may be extended under section 41EO.
41EN Notice of proposed suspension
(1) However, before suspending a conformity assessment certificate, the Secretary must:
(a) inform the person in writing that the Secretary proposes the suspension and set out the reasons for it; and
(b) give the person a reasonable opportunity to make submissions to the Secretary in relation to the proposed suspension.
(2) The Secretary is not to make a decision relating to the proposed suspension until the Secretary has had regard to any submissions the person makes under paragraph (1)(b).
(3) This section does not apply if the notice under section 41EM states that the suspension is necessary to prevent imminent risk of death, serious illness or serious injury.
41EO Duration of suspension
(1) The suspension takes effect:
(a) if the notice under section 41EM states that the suspension is necessary to prevent imminent risk of death, serious illness or serious injury—on the day on which the notice is given to the person; or
(b) in any other case—on the day specified for the purpose in the notice, being a day not earlier than 20 working days after the notice is given to the person.
(2) The suspension has effect until:
(a) the Secretary revokes it under section 41EP; or
(b) the expiry of:
(i) the period specified in the notice under section 41EM; or
(ii) if the period is extended under subsection (3) of this section, the period as so extended.
Note: Unless a suspension of a conformity assessment certificate has been revoked, the certificate is automatically revoked: see section 41ER.
(3) If a person in relation to whom a kind of medical device is included in the Register shows that he or she has taken steps to address the grounds for revoking the certificate under section 41ET, the Secretary may, by written notice given to the person, extend the period specified in the notice under section 41EM by a further specified period not exceeding 6 months.
41EP Revocation of suspension
(1) The Secretary must revoke the suspension if the Secretary is satisfied that:
(a) the ground on which the conformity assessment certificate was suspended no longer applies; and
(b) there are no other grounds for suspending the certificate.
(2) The Secretary’s power to revoke the suspension may be exercised:
(a) if:
(i) the manufacturer in relation to whom the conformity assessment certificate was issued; or
(ii) the person who applied for the certificate (if the applicant was not the manufacturer);
applies in writing to the Secretary; or
(b) on the Secretary’s own initiative.
(3) After revoking the suspension, the Secretary must, within 20 working days after the revocation, give written notice of the revocation to the person in relation to whom the conformity assessment certificate was issued.
(4) If the Secretary decides, after an application is made under paragraph (2)(a), not to revoke the suspension, the Secretary must:
(a) notify the applicant in writing of his or her decision within 20 working days after the decision is made; and
(b) state in the notice the reasons for the decision.
41EQ Powers of revocation of conformity assessment certificates unaffected
(1) This Division does not affect the Secretary’s powers to revoke a conformity assessment certificate under Division 4.
(2) To the extent that a suspension under this Division relates to a conformity assessment certificate to which such a revocation relates, the suspension ceases to have effect.
Division 4—Revocation of conformity assessment certificates
41ER Automatic revocation of conformity assessment certificates
The Secretary must, by written notice given to the person in relation to whom a conformity assessment certificate is issued, revoke the certificate if:
(a) the certificate has been suspended under section 41EM; and
(b) the period applying to the suspension under subsection 41EM(3) or 41EO(3) (as the case requires) expires before the suspension is revoked under section 41EP.
41ES Immediate revocation of conformity assessment certificates
(1) The Secretary may, by written notice given to the manufacturer in relation to whom a conformity assessment certificate is issued, revoke the certificate if the manufacturer requests in writing the revocation of the certificate.
(2) If:
(a) the Secretary revokes a certificate under subsection (1); and
(b) before the end of the period of 90 days beginning on the day the certificate was revoked, the manufacturer requests, in writing, the Secretary to withdraw the revocation; and
(c) the request is accompanied by the prescribed application fee (if any);
the Secretary may, by notice in writing given to the manufacturer, withdraw the revocation.
(3) If the revocation is withdrawn, the revocation is taken never to have occurred.
41ET Revocation of conformity assessment certificates after notice of proposed revocation
(1) The Secretary may, by written notice given to the person in relation to whom a conformity assessment certificate is issued, revoke the certificate if:
(a) the conformity assessment procedures have not been applied to medical devices of a kind to which the certificate applies; or
(b) the manufacturer in relation to whom the certificate is issued refuses or fails to comply with a condition to which the certificate is subject; or
(c) the Secretary gives to the person a notice under section 41JA that requires the person to give to the Secretary information or documents and the person fails to comply with that notice within a further 10 working days from the day specified in that notice; or
(d) the manufacturer in respect of whom the certificate is issued no longer manufactures any of the kinds of medical devices to which the certificate applies; or
(e) at least one of the following persons:
(i) the person (the holder) in relation to whom the certificate is issued;
(ii) a person (a manager) who makes, or participates in making, decisions that affect the whole, or a substantial part, of the holder’s affairs;
(iii) if the holder is a body corporate—a major interest holder of the body corporate;
has:
(iv) been convicted of an offence against this Act or a corresponding State law; or
(v) been convicted of an offence against a law of the Commonwealth or a law of a State or Territory involving fraud or dishonesty; or
(vi) been ordered to pay a pecuniary penalty for the contravention of a civil penalty provision of this Act or a corresponding State law; or
(vii) been ordered to pay a pecuniary penalty for the contravention of a civil penalty provision of a law of the Commonwealth or a law of a State or Territory involving fraud or dishonesty; or
(viii) breached a condition of a conformity assessment document; or
(ix) had a conformity assessment document suspended or revoked; or
(x) been a manager, or a major interest holder, of a body corporate in respect of which subparagraph (iv), (v), (vi), (vii), (viii) or (ix) applies, if the conduct resulting in that subparagraph applying occurred when the person was a manager or major interest holder of the body corporate; or
(f) any other circumstances prescribed by the regulations for the purposes of this paragraph exist.
(1A) A reference in paragraph (1)(e) to a person convicted of an offence includes a reference to a person in respect of whom an order has been made relating to the offence under:
(a) section 19B of the Crimes Act 1914; or
(b) a corresponding provision of a law of a State or Territory.
Note: Section 19B of the Crimes Act 1914 empowers a court that has found a person to have committed an offence to take action without proceeding to record a conviction.
(1B) Paragraph (1)(e) does not limit paragraph (1)(f).
(2) However, before revoking the certificate, the Secretary must:
(a) inform the person in writing that the Secretary proposes the revocation and set out the reasons for it; and
(b) give the person a reasonable opportunity to make submissions to the Secretary in relation to the proposed revocation.
(3) The Secretary is not to make a decision relating to the proposed revocation until the Secretary has had regard to any submissions the person makes under paragraph (2)(b).
(4) Nothing in this section affects the operation of Part VIIC of the Crimes Act 1914 (which includes provisions that, in certain circumstances, relieve persons from the requirement to disclose spent convictions and require persons aware of such convictions to disregard them).
41EU Limiting revocation of conformity assessment certificates to some medical devices of a particular kind
(1) If the Secretary is satisfied that the ground for revoking a conformity assessment certificate applies only to:
(a) some of the kinds of medical devices to which the certificate applies; or
(b) some medical devices of the kinds to which the certificate applies;
the Secretary must limit the revocation to the medical devices to which that ground or any other ground for revocation applies.
(2) If the revocation of the certificate is so limited, the Secretary must vary the certificate so that it no longer applies to the medical devices referred to in subsection (1).
41EV Publication of revocation etc. of conformity assessment certificates
The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after revoking a conformity assessment certificate, or varying a conformity assessment certificate under subsection 41EU(2), a notice setting out particulars of the revocation or variation.
41EW Date of effect of revocation etc. of conformity assessment certificates
If the Secretary revokes a conformity assessment certificate, or varies a conformity assessment certificate under subsection 41EU(2), the revocation or variation has effect:
(a) if the revocation is under section 41ER or 41ES, or the variation relates to a ground of revocation in section 41ER or 41ES—on the day on which the notice of revocation or variation is given to the person in relation to whom the certificate was issued; or
(b) in any other case—on such later day as is specified in the notice.
Part 4‑4A—Australian conformity assessment bodies
41EWA Conformity assessment body determinations
(1) The regulations may make provision for and in relation to empowering the Secretary to make conformity assessment body determinations.
(2) A conformity assessment body determination is a determination that a specified Australian corporation is an Australian conformity assessment body for the purposes of this Act.
(3) The regulations may make provision for and in relation to the following matters:
(a) applications for conformity assessment body determinations;
(b) the approval by the Secretary of a form for such an application;
(c) information that must accompany such an application;
(d) the application fee for such an application;
(e) the lapsing of such an application;
(f) the assessment by the Secretary of whether a conformity assessment body determination should be made in response to such an application;
(g) the assessment fee for such an assessment;
(h) the duration of conformity assessment body determinations.
(4) A conformity assessment body determination:
(a) may be of general application; or
(b) may be limited to either or both of the following:
(i) one or more specified medical devices;
(ii) one or more specified conformity assessment procedures.
(4A) If under the regulations the Secretary makes a conformity assessment body determination, the Secretary must assign a unique identification number to the body.
(4B) The Secretary must publish a list of the Australian conformity assessment bodies on the Department’s website.
(4C) The Secretary may also publish on the Department’s website any information relating to Australian conformity assessment bodies and either to conformity assessment body determinations or to certification‑related activities of Australian conformity assessment bodies.
(5) The regulations may provide that a conformity assessment body determination is subject to:
(a) the conditions prescribed by the regulations; and
(b) such other conditions (if any) as are specified in the determination.
Note: See subsections 41MN(10) to (12) and 41MNA(3) for offences and a civil penalty for a breach of the conditions.
(6) The following are examples of conditions that may be prescribed:
(a) a condition that the body will allow an authorised person:
(i) to enter, at any reasonable time, premises used by the body to carry on certification‑related activities; and
(ii) while on those premises, to inspect those premises and anything on those premises that concerns certification‑related activities carried on by the body; and
(iii) while on those premises, to make any still or moving image or any recording of those premises or anything on those premises that concerns certification‑related activities carried on by the body; and
(iv) while on those premises, to inspect, and make copies of, any documents that concern certification‑related activities carried on by the body;
(b) a condition that the body will, if requested to do so by the Secretary, give the Secretary information, or produce to the Secretary documents, that concern certification‑related activities carried on by the body.
(6A) The regulations may make provision for and in relation to the effect on an Australian conformity assessment body certificate of the Australian conformity assessment body ceasing to carry on certification‑related activities.
(6B) Without limiting subsection (6A), regulations made for the purposes of that subsection may make provision in relation to a matter by conferring on the Secretary a power to make a decision of an administrative character.
(7) The regulations may make provision for and in relation to empowering the Secretary to revoke, suspend or vary a conformity assessment body determination.
(7A) If under the regulations the Secretary suspends a conformity assessment body determination, the conditions referred to in subsection (5) continue during the suspension.
(8) Subsections (3) to (7) do not limit subsection (1).
(9) The express references in this section to the Secretary do not, by implication, prevent the regulations from empowering the Secretary to delegate any or all of the Secretary’s functions or powers under regulations made for the purposes of this section.
(10) If a conformity assessment body determination is in force under the regulations, the determination must be published on the Department’s website.
(11) A conformity assessment body determination made under the regulations is not a legislative instrument.
(12) Subsection 33(3AB) of the Acts Interpretation Act 1901 does not apply to the specification of an Australian corporation in a conformity assessment body determination.
Note: Subsection 33(3AB) of the Acts Interpretation Act 1901 deals with specification by class.
41EWB Content of Australian conformity assessment body certificates
(1) An Australian conformity assessment body certificate that is issued to a manufacturer of medical devices must specify whether it covers:
(a) all medical devices manufactured by the manufacturer; or
(b) only specified medical devices manufactured by the manufacturer.
(2) An Australian conformity assessment body certificate must contain any other information prescribed by the regulations for the purposes of this subsection.
(3) An Australian conformity assessment body certificate may be subject to conditions specified in the certificate.
41EWC Duration of Australian conformity assessment body certificates
(1) An Australian conformity assessment body certificate commences on the day specified for the purpose in the certificate. The certificate must specify the period for which it is to be in force (which must be no longer than 5 years).
(2) An Australian conformity assessment body certificate has effect at all times:
(a) unless the certificate is suspended by the Australian conformity assessment body; or
(b) until the end of the period specified in the certificate, or if the Australian conformity assessment body extends that period, until the end of that extended period; or
(c) until the certificate is revoked by the Australian conformity assessment body.
Extensions
(3) An Australian conformity assessment body that has issued an Australian conformity assessment body certificate may, in writing and on its own initiative, extend the period for which the certificate is in force.
(4) An extension must be no longer than 12 months.
(5) Only one extension may be given.
(6) The Australian conformity assessment body must give notice of an extension to the person to whom the certificate was issued.
41EWD Record‑keeping
(1) If an Australian corporation:
(a) is an Australian conformity assessment body; and
(b) is required by a condition referred to in subsection 41EWA(5) to keep records relating to certification‑related activities carried on by the corporation;
the Australian corporation must keep the records at all times while the corporation is an Australian conformity assessment body.
(2) If the Australian corporation ceases to be an Australian conformity assessment body, the corporation must keep the records referred to in subsection (1) for 15 years after that cessation.
Offences
(3) An Australian corporation commits an offence if:
(a) the corporation is subject to a requirement under this section; and
(b) the corporation contravenes the requirement.
Penalty: 1,200 penalty units.
(4) An Australian corporation commits an offence if:
(a) the corporation is subject to a requirement under this section; and
(b) the corporation contravenes the requirement.
Penalty: 300 penalty units.
(5) An offence against subsection (4) is an offence of strict liability.
Part 4‑5—Including medical devices in the Register
41F What this Part is about
Kinds of medical devices can be included in the Register if they comply with the essential principles, and conformity assessment procedures have been applied to the kinds of devices or requirements, comparable to those procedures, have been applied to the kinds of devices (and certain other requirements are complied with).
Inclusions in the Register are subject to certain automatic conditions and the Secretary may impose further conditions.
Division 1—Including medical devices in the Register
41FA What this Division is about
Kinds of medical devices are usually included in the Register once an application is made, together with the required certification and the application passes preliminary assessment. However, applications may be selected for audit, which involves checking some or all aspects of the application and certification.
Note 1: In some cases, an application relating to a kind of medical device will not pass preliminary assessment unless that kind of device is covered by a conformity assessment certificate under Part 4‑4: see paragraph 41FDB(2)(e).
Note 2: Dealing in medical devices of a kind not included in the Register may be an offence or may contravene a civil penalty provision: see Division 3 of Part 4‑11.
Subdivision A—Applications
41FC Making an application
(1) A person may make an application to the Secretary for a kind of medical device to be included in the Register.
(2) An application must not contain information that is false or misleading in a material particular.
Note: A person might also commit an offence, or contravene a civil penalty provision, if the person makes a statement in an application that is false or misleading in a material particular: see sections 41FE and 41FEA.
41FD Matters to be certified
The applicant must certify that:
(a) devices of the kind in question are medical devices; and
(b) devices of that kind are intended for a specified purpose, as ascertained under subsection 41BD(2); and
(c) the kind of device is correctly classified according to the medical device classifications; and
(d) devices of that kind comply with the essential principles; and
(e) the applicant:
(i) has available sufficient information to substantiate that compliance with the essential principles; or
(ii) has procedures in place, including a written agreement with the manufacturer of the kind of devices setting out the matters required by the regulations, to ensure that such information can be obtained from the manufacturer within the period specified in the regulations; and
(f) either:
(i) appropriate conformity assessment procedures have been applied to devices of that kind; or
(ii) requirements, comparable to the conformity assessment procedures, have been applied to devices of that kind; and
(g) the applicant:
(i) has available sufficient information to substantiate the application of the procedures referred to in subparagraph (f)(i) or the requirements referred to in subparagraph (f)(ii); or
(ii) has procedures in place, including a written agreement with the manufacturer of the kind of devices setting out the matters required by the regulations, to ensure that such information can be obtained from the manufacturer within the period specified in the regulations; and
(h) both of the following are complied with in relation to devices of that kind:
(i) the applicable provisions of the Therapeutic Goods Advertising Code;
(ii) the other requirements (if any) relating to advertising applicable under Part 5‑1 or under the regulations; and
(i) devices of that kind do not contain substances that are prohibited imports for the purposes of the Customs Act 1901; and
(ia) devices of that kind are not to be used exclusively for one or more of the purposes specified under section 41BEA; and
(j) the information included in or with the application is complete and correct.
Note: See section 41BH for when a medical device complies with the essential principles, section 41BI for when conformity assessment procedures are taken not to have been applied to a medical device and section 41BIA for when requirements comparable to those procedures are taken not to have been applied to a medical device.
41FDA Basis of certification of conformity assessment procedures
(1) When certifying the matter referred to in paragraph 41FD(f), the applicant must also state that the certification of the matter is based:
(a) on a conformity assessment certificate that is in force; or
(b) on an Australian conformity assessment body certificate that is in force; or
(c) on an overseas regulator conformity assessment document that is in force.
(2) However, subsection (1) does not apply if devices of the kind in question are class I medical devices (within the meaning of regulations made for the purposes of this Chapter).
41FDB Preliminary assessment of applications
(1) If an application is made under section 41FC for a kind of medical device to be included in the Register in relation to a person, the Secretary must carry out an assessment of whether the requirements set out in subsection (2) have been met in relation to the application.
(2) The requirements are as follows:
(a) the application must be made:
(i) in accordance with the form approved, in writing, by the Secretary for that classification of medical device; or
(ii) in such other manner as is approved, in writing, by the Secretary for that classification of medical device;
(b) the prescribed application fee for that classification of medical device must be paid;
(c) the application must be delivered to an office of the Department specified by the Secretary;
(d) the application must be accompanied by information that is:
(i) of a kind determined under subsection (7) for that classification of medical device; and
(ii) in a form determined under subsection (8) for that classification of medical device;
(e) if regulations made for the purposes of section 41EA require the manufacturer of the kind of device to have a conformity assessment certificate relating to the kind of medical device before an application under section 41FC can be made—such a certificate is in force;
(f) the applicant has certified the matters in section 41FD.
Passing preliminary assessment
(3) An application passes preliminary assessment if the Secretary:
(a) has carried out an assessment, under subsection (1), in relation to the application; and
(b) is satisfied that the requirements set out in subsection (2) have been met in relation to the application.
(4) If the application has not passed preliminary assessment, the Secretary must refuse the application.
Note: The Secretary is required to give notice of the refusal: see section 41FG.
Approval of forms etc.
(5) For the purposes of paragraph (2)(a), the Secretary may approve different forms and different manners for making applications for different medical device classifications.
(6) An approval of a form may require or permit an application or information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
Determination of kinds and forms of information
(7) The Secretary may, by legislative instrument, determine a kind of information for the purposes of the application of subparagraph (2)(d)(i) to medical devices of a particular classification.
(8) The Secretary may, by legislative instrument, determine a form of information for the purposes of the application of subparagraph (2)(d)(ii) to medical devices of a particular classification.
41FE Criminal offences for making a false statement
(1) A person commits an offence if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the person knows that the statement is false or misleading in a material particular; and
(c) the statement is in or in connection with:
(i) an application for including a kind of medical device in the Register under this Chapter; or
(ii) a certification or purported certification under section 41FD; and
(d) either:
(i) the use of the kind of medical device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the kind of medical device, if the kind of medical device were used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the person knows that the statement is false or misleading in a material particular; and
(c) the statement is in or in connection with:
(i) an application for including a kind of medical device in the Register under this Chapter; or
(ii) a certification or purported certification under section 41FD.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(5) A person commits an offence if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the statement is false or misleading in a material particular; and
(c) the statement is in or in connection with:
(i) an application for including a kind of medical device in the Register under this Chapter; or
(ii) a certification or purported certification under section 41FD.
Penalty: 100 penalty units.
(6) An offence against subsection (5) is an offence of strict liability.
41FEA Civil penalty for making a false statement
A person contravenes this section if:
(a) the person makes a statement (whether orally, in a document or in any other way); and
(b) the statement is false or misleading in a material particular; and
(c) the statement is in or in connection with:
(i) an application for including a kind of medical device in the Register under this Chapter; or
(ii) a certification or purported certification under section 41FD.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Subdivision B—Including kinds of medical devices in the Register
41FF Obligation to include kinds of medical devices in the Register
(1) If:
(a) an application for a kind of medical device to be included in the Register in relation to a person has passed preliminary assessment; and
(b) the application has not been selected for audit under section 41FH;
the Secretary must include the kind of device in the Register in relation to the person.
(1A) However, the Secretary must not include the kind of device in the Register in relation to the person if the Secretary is satisfied that the kind of device is to be used exclusively for one or more of the purposes specified under section 41BEA.
(2) As soon as practicable after the kind of device has been included in the Register, the Secretary must make available to the applicant a certificate of the inclusion of the kind of device in the Register.
(3) The certificate must specify the day on which the inclusion of the kind of device in the Register commences.
41FG Notification of unsuccessful applications
(1) This section applies if an application under subsection 41FC(1) for a kind of medical device to be included in the Register:
(a) is refused under subsection 41FDB(4); or
(b) is refused under subsection 41FF(1A).
(2) The Secretary must notify the applicant in writing, of the refusal within 20 working days after the application has been received and the prescribed application fee has been paid.
Subdivision C—Auditing of applications
41FH Selecting applications for auditing
(1A) This section applies to applications that have passed preliminary assessment.
(1) The Secretary:
(a) must select for auditing any application for a kind of medical device to be included in the Register that is an application of the kind prescribed by the regulations; and
(b) may select for auditing any other application for a kind of medical device to be included in the Register.
Note: An application audit assessment fee is payable in respect of any application that the Secretary must select for auditing: see Part 4‑10.
(2) If an application is selected for auditing:
(a) the Secretary must give the applicant a written notice (the selection notice) that:
(i) informs the applicant of the selection; and
(ii) requires the applicant to provide, within the period specified in the notice, information or documents that the Secretary is satisfied is relevant to the audit; and
(b) the application must be dealt with under this Subdivision and not under Subdivision B.
(3) The selection notice must be given within:
(a) 20 working days after the application is made and the prescribed application fee is paid; or
(b) if the regulations prescribe a longer period for that kind of application—that longer period.
(4) Subparagraph (2)(a)(ii) does not limit section 41JA (Secretary may require information).
41FI Auditing of applications
(1) In auditing the application, the Secretary may consider all or some aspects of one or both of the following matters:
(a) whether the application is in accordance with Subdivision A;
(b) whether matters as to which the applicant has certified under section 41FD are correct.
(1A) In auditing the application, the Secretary may, by written notice given to the applicant, require the applicant:
(a) to deliver to the office to which the application was made a reasonable number of samples of the kind of medical device to which the application relates within the period, of not less than 14 days after the day the notice is given, specified in the notice; and
(b) to do so in a manner specified in the notice.
(2) The Secretary must decide to include the kind of device to which the application relates in the Register, in relation to the person to whom the application relates, if the Secretary is satisfied as to all such aspects considered in the audit.
(3) The Secretary must decide not to include the kind of device to which the application relates in the Register if the Secretary is not so satisfied.
41FIA Certificates issued by Australian conformity assessment bodies
(1) If:
(a) a section 41FC application is made for a kind of medical device to be included in the Register; and
(b) the application has been selected for audit; and
(c) a person has obtained a certificate issued by an Australian conformity assessment body to the effect that the body is satisfied that an appropriate conformity assessment procedure has been applied to devices of that kind; and
(d) the certificate has been given to the Secretary; and
(e) if the conformity assessment body determination that relates to the body is limited as mentioned in paragraph 41EWA(4)(b)—the Secretary is satisfied that the certificate has been issued consistently with the determination;
the Secretary may have regard to the certificate in auditing the application.
(2) This section does not, by implication, limit the matters to which the Secretary may have regard.
41FJ Procedure following audits
After auditing the application, the Secretary must:
(a) notify the applicant in writing of his or her decision within 20 working days after the decision is made; and
(b) if the decision is not to include the kind of device to which the application relates in the Register—state in the notice the reasons for the decision; and
(c) if the decision is to include the kind of device in the Register and all assessment fees for the application that are due and payable have been paid:
(i) include the kind of device in the Register, in relation to the person in relation to whom the application was made; and
(ii) give the applicant a certificate of the inclusion of the kind of device in the Register.
41FK Lapsing of applications
An application that has been selected for auditing lapses if:
(a) the applicant fails to comply with a notice under section 41FH within 10 working days after the end of the period specified in the notice; or
(b) the applicant does not comply with a requirement by the Secretary under subsection 41FI(1A) to deliver to the office to which the application was made a reasonable number of samples of the kind of medical device to which the application relates; or
(c) the applicant fails to comply with a notice under section 41JA to give information relating to devices of that kind to the Secretary within a further 10 working days from the day specified in the notice; or
(d) information given to the Secretary by, or on behalf of, the applicant in connection with the application, including information given for the purpose of a requirement under section 41JA, is false or misleading in a material particular; or
(e) the applicant fails to pay an assessment fee for the application in accordance with section 41LB or 41LC.
Subdivision D—Miscellaneous
41FKA Medical devices (priority applicant) determinations
(1) The regulations may make provision for and in relation to empowering the Secretary to make medical devices (priority applicant) determinations.
(2) A medical devices (priority applicant) determination is a determination that, for the purposes of this Act, a specified person is a priority applicant in relation to any section 41FC application that may be made by the person for the inclusion in the Register of a medical device of a kind specified in the determination.
(3) The regulations may make provision for and in relation to the following matters:
(a) applications for medical devices (priority applicant) determinations;
(b) the approval by the Secretary of a form for such an application;
(c) information that must accompany such an application;
(d) the application fee for such an application;
(e) empowering the Secretary to give the applicant a written notice requiring the applicant to give to the Secretary specified information or documents in connection with the application within a specified period (which must be at least 10 working days after the notice is given to the applicant).
(4) The regulations may make provision for and in relation to the following matters:
(a) empowering the Secretary to revoke a medical devices (priority applicant) determination;
(b) the consequences of the revocation of a medical devices (priority applicant) determination.
(5) Subsections (3) and (4) do not limit subsection (1).
(6) The regulations may make provision for and in relation to the priority to be given by the Secretary to consideration of a section 41FC application where the applicant is a priority applicant.
(7) The regulations may provide that, if:
(a) a person is a priority applicant in relation to a section 41FC application made by the person; and
(b) a decision is made on the application;
a statement setting out the decision may be published on the Department’s website.
(8) The express references in this section to the Secretary do not, by implication, prevent the regulations from empowering the Secretary to delegate any or all of the Secretary’s functions or powers under regulations made for the purposes of this section.
(9) If a medical devices (priority applicant) determination is in force under the regulations, the determination may be published on the Department’s website.
(10) A medical devices (priority applicant) determination made under the regulations is not a legislative instrument.
(11) Subsection 33(3AB) of the Acts Interpretation Act 1901 does not apply to the specification of a person in a medical devices (priority applicant) determination.
Note: Subsection 33(3AB) of the Acts Interpretation Act 1901 deals with specification by class.
41FL Device number
If a kind of medical device is included in the Register, the Secretary is to assign a unique device number to it.
41FM Duration of inclusion in the Register
(1) The inclusion of a kind of medical device in the Register commences on the day specified for the purpose in the certificate under section 41FF or 41FJ.
(2) The inclusion of a kind of medical device in the Register has effect at all times:
(a) unless the kind of device is suspended from the Register under Division 1 of Part 4‑6; or
(b) until entry of the kind of device is cancelled from the Register under Division 2 of Part 4‑6.
Division 2—Conditions
Note: Breaching conditions of the inclusion of a kind of medical device may lead to suspension or cancellation of the entry of the kind of device from the Register (see Part 4‑6), may be an offence (see subsections 41MN(1), (4) and (4A)), and may contravene a civil penalty provision (see subsection 41MNA(1)).
41FN Conditions applying automatically
Entry and inspection powers
(1) The inclusion of a kind of medical device in the Register is subject to the conditions that the person in relation to whom the kind of device is included in the Register will:
(a) allow an authorised person:
(i) to enter, at any reasonable time, any premises (including premises outside Australia) at which that person or any other person deals with medical devices of that kind; and
(ii) while on those premises, to inspect those premises and medical devices of any kind on those premises and to examine, take measurements of, conduct tests on, require tests to be conducted on or take samples of medical devices of any kind on those premises or any thing on those premises that relates to medical devices of any kind; and
(iii) while on those premises, to make any still or moving image or any recording of those premises or any thing on those premises; and
(b) if requested to do so by an authorised person, produce to the person such documents relating to devices of the kind included in the Register as the person requires and allow the person to copy the documents.
Delivery of samples
(2) The inclusion of a kind of medical device in the Register is subject to a condition that the person in relation to whom the kind of device is included in the Register will deliver a reasonable number of samples of the kind of device if the Secretary so requests:
(a) within the period specified in the request; and
(b) in accordance with any other requirements specified in the request.
The period specified in the request must include at least 10 working days.
Availability etc. of information
(3) The inclusion of a kind of medical device in the Register is subject to conditions that:
(a) at all times while the inclusion in the Register has effect, the person in relation to whom the kind of device is included in the Register:
(i) has available sufficient information to substantiate compliance with the essential principles; or
(ii) has procedures in place, including a written agreement with the manufacturer of the kind of devices setting out the matters required by the regulations, to ensure that such information can be obtained from the manufacturer within the period specified in the regulations; and
(b) at all times while the inclusion in the Register has effect, the person in relation to whom the kind of device is included in the Register:
(i) has available sufficient information to substantiate that the conformity assessment procedures have been applied to the kind of medical device or that requirements, comparable to those procedures, have been applied to the kind of medical device to the satisfaction of an overseas regulator; or
(ii) has available information relating to changes to the kind of medical device, the product range, and quality management system, of the manufacturer of the device; or
(iii) has procedures in place, including a written agreement with the manufacturer of the kind of devices setting out the matters required by the regulations, to ensure that such information can be obtained from the manufacturer within the period specified in the regulations; and
(c) at any time while the inclusion in the Register has effect, the person in relation to whom the kind of device is included in the Register will, if asked to do so by the Secretary, give the information to the Secretary; and
(d) the person in relation to whom the kind of device is included in the Register will give information of a kind mentioned in subsection 41MP(2) or 41MPA(2) to the Secretary within the period specified in the regulations; and
(e) the person in relation to whom the kind of device is included in the Register will give the manufacturer of the kind of medical device information relevant to:
(i) the manufacturer’s obligations under the conformity assessment procedures or requirements comparable to those procedures; and
(ii) whether medical devices of that kind comply with the essential principles.
(4) The regulations may prescribe the amount, standard or kind of information or evidence required for the purposes of paragraphs (3)(c), (d) and (e).
Advertising material
(5) The inclusion of a kind of medical device in the Register is subject to a condition that advertising material relating to medical devices of that kind is consistent with the intended purpose as certified under section 41FD.
Conditions prescribed by the regulations
(5A) The inclusion of a kind of medical device in the Register is subject to such conditions (if any) as are prescribed by the regulations.
Conditions determined by the Minister
(5B) The inclusion of a kind of medical device in the Register is subject to such conditions (if any) as are determined under subsection (5C).
(5C) The Minister may, by legislative instrument, determine one or more conditions for the purposes of subsection (5B).
Conditions do not limit other conditions
(6) A condition imposed under this section is in addition to any conditions imposed under this Division.
41FO Conditions imposed when kinds of medical devices are included in the Register
(1) If the Secretary includes a kind of medical device in the Register in relation to a person, the Secretary may, in writing, impose conditions on the inclusion of the kind of device in the Register.
(2) Conditions referred to in subsection (1) may relate to:
(a) manufacture of devices of that kind; or
(b) custody, intended purpose, supply, disposal or destruction of devices of that kind; or
(c) keeping of records relating to devices of that kind, including records relating to the tracking and location of devices of that kind after their supply; or
(d) matters dealt with in, or matters additional to matters dealt with in, the essential principles; or
(e) such other matters relating to devices of that kind as the Secretary thinks appropriate.
41FP Conditions imposed after kinds of medical devices are included in the Register
(1) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register:
(a) impose new conditions on including the kind of device in the Register under this Chapter; or
(b) vary or remove existing conditions.
The power may be exercised at the person’s request or on the Secretary’s own initiative.
(2) The imposition, variation or removal of a condition under this section takes effect:
(a) if the notice states that the action is necessary to prevent imminent risk of death, serious illness or serious injury—on the day on which the notice is given to the person; or
(aa) in the case of an imposition or variation requested by the person, and to which paragraph (a) does not apply—on the day specified in the notice, which must be at least 20 working days after the notice is given to the person, unless the person has agreed to an earlier day; or
(ab) in the case of a removal to which paragraph (a) does not apply—on the day specified in the notice, which must be at least 20 working days after the notice is given to the person, unless the person has agreed to an earlier day; or
(b) in any other case—on the day specified for the purpose in the notice, being a day not earlier than 20 working days after the notice is given to the person.
(3) For the purposes of paragraphs (2)(aa) and (ab), the earlier day must not be earlier than the day the notice is given to the person.
Part 4‑6—Suspension and cancellation from the Register
Division 1—Suspension from the Register
Subdivision A—General power of suspension
41G What this Part is about
Inclusions in the Register may be suspended in certain circumstances, such as when a conformity assessment document is suspended. A kind of medical device that is suspended is taken not to be included in the Register for most purposes.
Inclusions in the Register may also be cancelled in certain circumstances.
41GA Suspension of kinds of medical devices from the Register
(1) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, suspend the kind of device from the Register if:
(a) the Secretary is satisfied that:
(i) there is a potential risk of death, serious illness or serious injury if the kind of device continues to be included in the Register; and
(ii) it is likely that the person will, within the period of the suspension, be able to take the action necessary to ensure that the kind of device would not cause a potential risk of death, serious illness or serious injury if it were to continue to be included in the Register; or
(b) the Secretary is satisfied that it is likely that there are grounds for cancelling the entry of the kind of device from the Register under Division 2 (other than under paragraph 41GL(a), (d) or (f) or section 41GM).
(2) The suspension may be limited to some medical devices of that kind, as specified in the notice.
(3) The notice must specify the period of the suspension. The period must not exceed 6 months.
Note: The period of the suspension may be extended under section 41GC.
(4) The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after the suspension, a notice setting out particulars of the suspension.
41GB Notice of proposed suspension must be given in certain cases
(1) However, before suspending a kind of medical device from the Register because it is likely that there are grounds for cancelling the entry of the kind of device from the Register under section 41GN, the Secretary must:
(a) inform the person by written notice that the Secretary proposes the suspension and set out the reasons for it; and
(b) give the person a reasonable opportunity to make submissions to the Secretary in relation to the proposed suspension.
(2) The Secretary is not to make a decision relating to the proposed suspension until the Secretary has had regard to any submissions the person makes under paragraph (1)(b).
41GC Duration of suspension
(1) The suspension takes effect:
(a) if the notice under subsection 41GA(1) states that the suspension is necessary to prevent a potential risk of death, serious illness or serious injury—on the day on which the notice is given to the person; or
(b) in any other case—on the day specified for the purpose in the notice, being a day not earlier than 20 working days after the notice is given to the person.
(2) The suspension has effect until:
(a) the Secretary revokes it under section 41GD; or
(b) the end of:
(i) the period specified in the notice under subsection 41GA(3); or
(ii) if the period is extended under subsection (3) of this section, the period as so extended.
Note: Unless a suspension of a kind of medical device has been revoked, the entry of the kind of medical device is automatically cancelled from the Register: see section 41GK.
(3) If a person in relation to whom a kind of medical device is included in the Register shows that he or she has taken steps to remove the grounds for cancelling the entry of the kind of device from the Register under section 41GN, the Secretary may, by written notice given to the person, extend the period specified in the notice under subsection 41GA(1) by a further specified period not exceeding 6 months.
(4) The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after the extension, a notice setting out particulars of the extension.
41GD Revocation of suspension
(1) The Secretary must revoke the suspension if the Secretary is satisfied that:
(a) the ground on which the kind of medical device concerned was suspended from the Register no longer applies; and
(b) there are no other grounds for suspending the kind of device from the Register.
(2) The Secretary’s power to revoke the suspension may be exercised:
(a) if the person in relation to whom the kind of medical device concerned is included in the Register applies in writing to the Secretary; or
(b) on the Secretary’s own initiative.
(3) After revoking the suspension, the Secretary must:
(a) within 20 working days after the revocation, give written notice of the revocation to the person in relation to whom the kind of medical device concerned is included in the Register; and
(b) as soon as practicable after the revocation, cause to be published in the Gazette or on the Department’s website a notice setting out particulars of the revocation.
(4) If the Secretary decides, after an application is made under paragraph (2)(a), not to revoke the suspension, the Secretary must:
(a) notify the applicant in writing of his or her decision within 20 working days after the decision is made; and
(b) state in the notice the reasons for the decision.
41GE Treating applications for revocation as having been refused
(1) The applicant for the suspension to be revoked may give the Secretary written notice that the applicant wishes to treat the application as having been refused if:
(a) a period is prescribed under paragraph 63(2)(dd) for the Secretary to make a decision on the application; and
(b) at the end of the period, the Secretary has not made a decision.
(2) The notice may be given at any time before the Secretary makes a decision on the application.
(3) If a notice has been given, this Act (except for subsection 60(5)) has effect as if:
(a) the Secretary had decided not to revoke the suspension; and
(b) the Minister had made a decision under subsection 60(3) confirming the decision of the Secretary; and
(c) the Minister’s decision had been made on the day on which notice was given to the Secretary.
Subdivision B—Suspension as a result of suspension of conformity assessment document
41GF Suspension where conformity assessment certificate suspended
(1) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, suspend the kind of device from the Register if the conformity assessment certificate applying to that kind of device is suspended under Division 3 of Part 4‑4.
(2) If the suspension under Division 3 of Part 4‑4 is limited to some medical devices of that kind, the suspension under this section is taken to be limited to the same extent.
(3) The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after the suspension, a notice setting out particulars of the suspension.
41GFA Suspension where other certificates or documents are suspended
(1) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, suspend the kind of device from the Register if:
(a) an Australian conformity assessment body certificate that applies to the kind of device is suspended by the Australian conformity assessment body; or
(b) an overseas regulator conformity assessment document that applies to the kind of device is suspended by the overseas regulator.
(2) However, before suspending the kind of device from the Register, the Secretary must:
(a) inform the person in writing that the Secretary proposes the suspension and set out the reasons for it; and
(b) give the person a reasonable opportunity to make submissions to the Secretary in relation to the proposed suspension.
(3) The Secretary is not to make a decision relating to the proposed suspension until the Secretary has had regard to any submissions the person makes under paragraph (2)(b).
(4) The Secretary must cause to be published on the Department’s website, as soon as practicable after the suspension, a notice setting out particulars of the suspension.
41GG Duration of suspension
(1) A suspension under section 41GF or 41GFA takes effect on the day on which the notice is given to the person.
(2) The suspension has effect until the Secretary revokes it under section 41GH.
41GH Revocation of suspension
(1) The Secretary must revoke a suspension under section 41GF if:
(a) the suspension under Division 3 of Part 4‑4 ceases to have effect; and
(b) the Secretary is satisfied that there are no other grounds for suspending the kind of device from the Register.
(1A) The Secretary may revoke a suspension under section 41GFA if:
(a) either:
(i) the suspension referred to in paragraph 41GFA(1)(a) or (b) ends; or
(ii) the person in relation to whom the kind of medical device is included in the Register provides the Secretary with another conformity assessment document that applies to the kind of device; and
(b) the Secretary is satisfied that there are no other grounds for suspending the kind of device from the Register.
(2) After making a revocation under subsection (1) or (1A), the Secretary must:
(a) within 20 working days after the revocation, give written notice of the revocation to the person in relation to whom the kind of medical device concerned is included in the Register; and
(b) as soon as practicable after the revocation, cause to be published in the Gazette or on the Department’s website a notice setting out particulars of the revocation.
Subdivision C—Effect of suspension
41GI Effect of suspension
If all or some medical devices of a particular kind are suspended, they are taken, for the purposes of this Act (other than Division 2 of Part 4‑5, this Division and Part 4‑8), not to be included in the Register while the suspension has effect.
Note: Dealing in medical devices that are not included in the Register may be an offence or may contravene a civil penalty provision: see Division 3 of Part 4‑11.
41GJ Powers of cancellation from Register unaffected
(1) This Subdivision does not affect the Secretary’s powers to cancel the entry of kinds of medical devices from the Register under Division 2.
(2) To the extent that a suspension under this Division relates to medical devices to which such a cancellation relates, the suspension ceases to have effect.
Division 2—Cancellation of entries from the Register
41GK Automatic cancellation of entries of kinds of medical devices from the Register
The Secretary must, by written notice given to the person in relation to whom a kind of medical device is included in the Register, cancel the entry of the kind of device from the Register if:
(a) the kind of device has been suspended from the Register under section 41GA, and the period applying to the suspension under subsection 41GA(3) or 41GC(3) (as the case requires) expires before the suspension is revoked under section 41GD; or
(b) a conformity assessment certificate applying to that kind of device is revoked under Division 4 of Part 4‑4.
41GL Immediate cancellation of entries of kinds of medical devices from the Register
The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, cancel the entry of the kind of device from the Register if:
(a) the Secretary is satisfied that there would be an imminent risk of death, serious illness or serious injury if the kind of device continues to be included in the Register; or
(b) devices of that kind are no longer therapeutic goods; or
(c) devices of that kind are no longer medical devices; or
(ca) the kind of medical device is covered by an exemption under paragraph 41HA(1)(b); or
(d) the person requests in writing the cancellation of the entry of the kind of device from the Register; or
(e) the Secretary is satisfied that a statement made in or in connection with:
(i) the application for including the kind of device in the Register; or
(ii) the certification or purported certification under section 41FD relating to the application;
was false or misleading in a material particular; or
(f) the annual charge payable under subsection 4(1B) of the Therapeutic Goods (Charges) Act 1989 in respect of the inclusion of the kind of device in the Register is not paid within 20 working days after it becomes payable; or
(g) the person contravenes a direction, or a condition of a direction, given to the person under subsection 42DV(1) in relation to the advertising of the kind of device and the Secretary is satisfied that the contravention is significant; or
(ga) if the person is a body corporate—a related body corporate of the person contravenes a direction, or a condition of a direction, given to the related body corporate under subsection 42DV(1) in relation to the advertising of the kind of device and the Secretary is satisfied that the contravention is significant; or
(h) there is a breach, involving the kind of device, of an applicable provision of the Therapeutic Goods Advertising Code or any other requirement relating to advertising applicable under Part 5‑1 or under the regulations, and the Secretary is satisfied that:
(i) the breach is significant; and
(ii) as a result of the breach, the presentation of devices of that kind is misleading to a significant extent.
41GLA Revocation of cancellation of entries upon request
(1) If:
(a) the Secretary cancels the entry of a kind of medical device because of the request of a person made under paragraph 41GL(d); and
(b) before the end of the period of 90 days beginning on the day the kind of device ceased to be included in the Register, the person requests, in writing, the Secretary to revoke the cancellation; and
(c) the request is accompanied by the prescribed application fee (if any);
the Secretary may, by notice in writing given to the person, revoke the cancellation.
(2) If the cancellation is revoked, the cancellation is taken never to have occurred.
41GLB Revocation of cancellation of entries—payment of annual charge
(1) If:
(a) the Secretary cancels the entry of a kind of medical device because the annual charge payable by a person under subsection 4(1B) of the Therapeutic Goods (Charges) Act 1989 in respect of the inclusion of the kind of device in the Register was not paid within 20 working days after it becomes payable; and
(b) before the end of the period of 90 days beginning on the day the kind of device ceased to be included in the Register, the person in relation to whom the kind of device was included in the Register requests, in writing, the Secretary to revoke the cancellation; and
(c) the annual charge payable under subsection 4(1B) of the Therapeutic Goods (Charges) Act 1989 in respect of the inclusion of the kind of device in the Register has been paid; and
(d) the request is accompanied by the prescribed application fee (if any);
the Secretary may, by notice in writing given to the person, revoke the cancellation.
(2) If the cancellation is revoked, the cancellation is taken never to have occurred.
41GM Cancellation of entries of kinds of medical devices from the Register after section 41JA notice
(1) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, cancel the entry of the kind of device from the Register if:
(a) the Secretary gives to the person a notice under section 41JA requiring the person to give to the Secretary information or documents relating to the kind of device; and
(b) the notice under section 41JA is given for the purposes of ascertaining whether any of the certifications by the person under section 41FD in relation to the kind of device are incorrect; and
(c) the person fails to comply with the notice under section 41JA within a further 10 working days from the day specified in that notice.
(2) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, cancel the entry of the kind of device from the Register if:
(a) the Secretary gives to the person a notice under section 41JA requiring the person to give to the Secretary information or documents relating to whether medical devices of that kind are being:
(i) supplied in Australia; or
(ii) imported into Australia; or
(iii) exported from Australia; and
(b) either:
(i) the information or documents given are to the effect that medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia; or
(ii) the person fails to comply with the notice under section 41JA within a further 10 working days from the day specified in that notice.
41GN Cancellation of entries of kinds of medical devices from the Register after notice of proposed cancellation
(1) The Secretary may, by written notice given to the person in relation to whom a kind of medical device is included in the Register, cancel the entry of the kind of device from the Register if:
(a) medical devices that were devices of that kind when the kind of device was included in the Register have changed so those medical devices are no longer devices of that kind; or
(b) the person in relation to whom the kind of medical device is included in the Register refuses or fails to comply with a condition to which that inclusion is subject; or
(c) the Secretary gives to the person a notice under section 41JA:
(i) that requires the person to give to the Secretary information or documents relating to the kind of device; and
(ii) in respect of which section 41GM does not apply;
and the person fails to comply with that notice within a further 10 working days from the day specified in that notice; or
(d) the person contravenes subsection 41MP(1) or 41MPA(1) in relation to the kind of device; or
(e) the Secretary is satisfied that the safety or performance of the kind of device is unacceptable; or
(f) the Secretary is satisfied that any certification, or part of a certification, under section 41FD in relation to the application for inclusion of the kind of device in the Register is incorrect, or is no longer correct, in a material particular; or
(g) a conformity assessment document that applies to the kind of device expires; or
(h) either of the following applies:
(i) an Australian conformity assessment body certificate that applies to the kind of device is revoked by the Australian conformity assessment body;
(ii) an overseas regulator conformity assessment document that applies to the kind of device is revoked by the overseas regulator; or
(i) the person contravenes a direction, or a condition of a direction, given to the person under subsection 42DV(1) in relation to the advertising of the kind of device; or
(j) if the person is a body corporate—a related body corporate of the person contravenes a direction, or a condition of a direction, given to the related body corporate under subsection 42DV(1) in relation to the advertising of the kind of device; or
(k) either of the following has not been complied with in relation to the kind of device:
(i) an applicable provision of the Therapeutic Goods Advertising Code;
(ii) any other requirement relating to advertising applicable under Part 5‑1 or the regulations.
(2) However, before cancelling the entry of the kind of device from the Register, the Secretary must:
(a) inform the person in writing that the Secretary proposes the cancellation and set out the reasons for it; and
(b) give the person a reasonable opportunity to make submissions to the Secretary in relation to the proposed cancellation.
(3) The Secretary is not to make a decision relating to the proposed cancellation until the Secretary has had regard to any submissions the person makes under paragraph (2)(b).
41GO Limiting cancellation of entries from Register to some medical devices of a particular kind
(1) If the Secretary is satisfied that the ground for cancelling the entry of a kind of medical device from the Register applies only to some medical devices of that kind, the Secretary must limit the cancellation to the medical devices to which that ground or any other ground for cancellation applies.
(2) If the cancellation of the entry of a kind of medical device from the Register is limited to some medical devices of that kind, the Secretary:
(a) must vary the entry in the Register accordingly; and
(b) must not delete the entry from the Register because of the cancellation.
41GP Publication of cancellation of entry from Register
The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after cancelling an entry from the Register of a kind of medical device, or of some devices of a particular kind, a notice setting out particulars of the cancellation.
41GQ Date of effect of cancellation of entries from Register
If the Secretary cancels an entry of a kind of medical device, or some devices of a particular kind, from the Register, the cancellation has effect:
(a) if the cancellation is under section 41GK or 41GL—on the day on which the notice of cancellation is given to the person in relation to whom the kind of device was included in the Register; or
(b) in any other case—on such later day as is specified in the notice, being a day not earlier than 20 working days after the notice is given to the person.
Part 4‑6A—Exempting medical devices to deal with emergencies
41GR What this Part is about
The Minister may exempt certain medical devices from various provisions of this Chapter so that the devices may be stockpiled to deal with possible future emergencies or made available urgently to deal with actual emergencies.
Note 1: There are offences and civil penalty provisions related to the making of exemptions under this Part: see Division 3A of Part 4‑11.
Note 2: Some of the other provisions of this Act about medical devices exempt under this Part are:
(a) section 41JCA (providing information to the Secretary); and
(b) section 41KA (public notification and recall of medical devices); and
(c) section 46A (search of premises).
41GS Minister may make exemptions
(1) The Minister may, by writing, exempt specified kinds of medical devices from the operation of the following:
(a) Division 1 of Part 4‑2 (essential principles);
(b) Division 1 of Part 4‑3 (conformity assessment procedures);
(c) Part 4‑4 (conformity assessment certificates);
(d) Part 4‑5 (including medical devices in the Register).
(2) The Minister may make an exemption under subsection (1) only if the Minister is satisfied that, in the national interest, the exemption should be made so that:
(a) the devices may be stockpiled as quickly as possible in order to create a preparedness to deal with a potential threat to public health that may be caused by a possible future emergency; or
(b) the devices can be made available urgently in Australia in order to deal with an actual threat to public health caused by an emergency that has occurred.
Period of exemption
(3) An exemption under subsection (1) comes into force:
(a) on the day the exemption is made; or
(b) on a later day specified in the exemption.
(4) An exemption under subsection (1) remains in force for the period specified in the exemption, unless revoked earlier.
Note: Section 41GU deals with variation and revocation of the exemption.
Effect of inclusion of kind of medical device in the Register
(5) An exemption under subsection (1) ceases to have effect in relation to a particular kind of medical device when that kind of medical device becomes included in the Register under Part 4‑5.
Exemption not a legislative instrument
(6) An exemption under subsection (1) is not a legislative instrument.
Disregard section 41BE
(7) For the purposes of this Act, disregard section 41BE in working out the kinds of medical devices covered by an exemption under subsection (1) of this section.
41GT Conditions of exemptions
An exemption under section 41GS is subject to conditions specified in the exemption about any of the following:
(a) the quantity of medical devices that are exempt;
(b) the source of those medical devices;
(c) the persons or class of persons who may import, manufacture, supply or export those medical devices;
(d) the supply of those medical devices (including the persons or class of persons to whom medical devices may be supplied for use and the circumstances under which a stockpile of medical devices may be supplied for use);
(e) the storage and security of those medical devices;
(f) the keeping and disclosure of, and access to, records about those medical devices;
(g) the disposal of those medical devices;
(h) the manner in which any of those medical devices are to be dealt with if a condition of the exemption is breached;
(i) any other matters that the Minister thinks appropriate.
Whether or not medical devices are exempt under section 41GS is not affected by whether or not there is a breach of a condition under this section in relation to those medical devices.
Note 1: There are offences and civil penalty provisions related to the breach of a condition of an exemption: see Division 3A of Part 4‑11.
Note 2: Section 41GU deals with variation and revocation of the conditions.
41GU Variation or revocation of exemption
Variation of exemption
(1) The Minister may, by writing, vary an exemption made under section 41GS by removing specified kinds of medical devices from the exemption.
Revocation of exemption
(2) The Minister may, by writing, revoke an exemption made under section 41GS.
Variation or revocation of conditions
(3) The Minister may, by writing:
(a) vary the conditions of an exemption made under section 41GS (including by imposing new conditions); or
(b) revoke the conditions of an exemption made under section 41GS.
When variation or revocation takes effect
(4) A variation or revocation under this section takes effect:
(a) if the Minister states in the variation or revocation that the variation or revocation is necessary to prevent imminent risk of death, serious illness or serious injury—on the day the variation or revocation is made; or
(b) in any other case—on a later day specified in the variation or revocation (which must not be earlier than 28 days after the day the variation or revocation is made).
41GV Informing persons of exemption etc.
If the Minister makes an exemption under section 41GS, the Minister must take reasonable steps to give a copy of the following to each person covered by paragraph 41GT(c):
(a) the exemption;
(b) any variation or revocation of the exemption under section 41GU.
41GW Notification and tabling
Notification
(1) The Secretary must cause a notice setting out particulars of the following:
(a) an exemption made under section 41GS because of paragraph 41GS(2)(b);
(b) a variation or revocation under section 41GU, to the extent that the variation or revocation relates to an exemption made under section 41GS because of paragraph 41GS(2)(b);
to be published in the Gazette within 5 working days after the day on which the exemption, variation or revocation is made. However, the exemption, variation or revocation is not invalid merely because of a failure to comply with this subsection.
Tabling
(2) The Minister must cause a document setting out particulars of the following:
(a) an exemption made under section 41GS because of paragraph 41GS(2)(b);
(b) a variation or revocation under section 41GU, to the extent that the variation or revocation relates to an exemption made under section 41GS because of paragraph 41GS(2)(b);
to be tabled in each House of the Parliament within 5 sitting days of that House after the day on which the exemption, variation or revocation is made. However, the exemption, variation or revocation is not invalid merely because of a failure to comply with this subsection.
41GY Disposal of unused medical devices
(1) This section applies to a medical device if:
(a) an exemption under section 41GS in relation to that kind of medical device ceases to have effect otherwise than because that kind of medical device becomes included in the Register under Part 4‑5; and
(b) the medical device has not been used before the exemption so ceases to have effect.
(2) The Secretary may arrange for the disposal of the medical device in accordance with the regulations.
(3) Regulations made for the purposes of subsection (2) may set out the methods by which the medical device is to be stored, supplied, destroyed, exported or otherwise disposed of.
(4) A method set out in the regulations under subsection (3) must not enable or permit any benefit to be conferred on a person (including the Commonwealth) other than the owner of the medical device.
Part 4‑7—Other exemptions from including medical devices in the Register
41H What this Part is about
In addition to Part 4‑6A, there are 4 other kinds of exemptions from the prohibitions in Division 3 of Part 4‑11 on dealing in medical devices that are not included in the Register:
(a) medical devices exempted under the regulations;
(b) approval for medical devices to be used for special treatment of individuals or for experimental purposes;
(c) authorisation of health practitioners to supply specified medical devices;
(d) medical devices exempted if substitutes are unavailable or in short supply.
41HA Devices exempted from inclusion in the Register
(1) The regulations may exempt from the operation of Division 3 of Part 4‑11:
(a) all medical devices, except those medical devices of the kinds prescribed for the purposes of this paragraph; or
(b) specified kinds of medical devices.
Note: Division 3 of Part 4‑11 contains offences and civil penalty provisions relating to dealing in medical devices that are not included in the Register.
(2) An exemption may be subject to conditions that are prescribed in the regulations.
Note: Breach of the conditions may be an offence: see subsection 41MN(9).
(3) An exemption under paragraph (1)(a) has effect only for classes of persons prescribed in the regulations for the purposes of this subsection.
(4) If the regulations revoke an exemption, the revocation takes effect on the day specified. The day must not be earlier than 20 working days after the day on which the regulations are made.
41HB Exemptions for special and experimental uses
(1) The Secretary may grant a written approval to a person for:
(a) the importation into Australia; or
(b) the exportation from Australia; or
(c) the supply in Australia;
of a specified medical device or kind of medical device (other than medical devices included in the Register or exempt devices):
(d) for use in the treatment of another person; or
(e) for use solely for experimental purposes in humans.
Note: For variation of an approval for use of the kind referred to in paragraph (1)(e), see subsection (8).
(1A) An approval for use of the kind referred to in paragraph (1)(d) must not be granted to a person unless the person is a health practitioner.
(2) The approval may be given subject to conditions specified in the approval, including a condition relating to charging for medical devices of the kinds in question.
Note: Breach of the conditions may be an offence: see subsection 41MN(9).
(3) In addition, the regulations may prescribe conditions that apply to a person’s approval to use specified kinds of medical devices solely for experimental purposes in humans. The conditions may relate to one or more of the following:
(a) the preconditions on another person’s use of devices of those kinds for those purposes;
(b) the principles to be followed in another person’s use of devices of those kinds for those purposes;
(c) the monitoring of another person’s use, and the results of that use, of devices of those kinds for those purposes;
(d) the circumstances in which that other person must cease using devices of those kinds for those purposes.
(4) An application to use specified medical devices in the treatment of another person must be in a form (if any) approved, in writing, by the Secretary and be accompanied by any information about the devices that is required by the Secretary.
(5) An application to use specified kinds of medical devices solely for experimental purposes in humans must:
(a) be in a form (if any) approved, in writing, by the Secretary; and
(b) be accompanied by any information about the kinds of devices that is required by the Secretary; and
(c) be accompanied by the prescribed fee.
(6) The Secretary must:
(a) consider any application under this section; and
(b) assess any information submitted with the application; and
(c) notify the applicant, within 20 working days of making the decision:
(i) of the decision; and
(ii) in the case of a decision not to grant the approval—of the reasons for the decision.
(7) The use by a person for experimental purposes in humans of specified kinds of medical devices that are the subject of an approval granted to someone else under paragraph (1)(e) is subject to the conditions (if any) specified in the regulations relating to one or more of the following:
(a) the preconditions on the use of devices of those kinds for those purposes;
(b) the principles to be followed in the use of devices of those kinds for those purposes;
(c) the monitoring of the use, and the results of the use, of devices of those kinds for those purposes;
(d) the circumstances in which the person must cease the use of devices of those kinds for those purposes.
Note: Breach of the conditions may be an offence: see subsection 41MN(9).
Varying approval for use solely for experimental purposes in humans
(8) If:
(a) the Secretary grants an approval to a person under subsection (1) for use of the kind referred to in paragraph (1)(e); and
(b) the person requests the Secretary to do either or both of the following:
(i) vary the medical device or kind of medical device specified in the approval;
(ii) vary the conditions imposed under subsection (2) on the approval; and
(c) the request is in a form (if any) approved, in writing, by the Secretary; and
(d) the request is accompanied by such information relating to the medical device or kind of medical device as is required by the Secretary; and
(e) the request is accompanied by the fee prescribed by the regulations;
the Secretary must, by notice in writing, vary or refuse to vary the approval. Any variation may be different than the variation requested and may involve imposing new conditions on the approval or varying or removing existing conditions.
(9) The Secretary must notify the person making the request under subsection (8) of:
(a) the Secretary’s decision on the request; and
(b) for a decision to vary the approval in a way that is different than the variation requested or a decision to refuse to vary the approval—the reasons for the decision.
(10) A variation under subsection (8) takes effect at the time the Secretary notifies the person under subsection (9) of the variation.
41HC Authorities for health practitioners
(1) The Secretary may authorise, in writing, a specified medical practitioner to supply specified kinds of medical devices for use in the treatment of humans to a specified class of recipients.
(1A) An application for an authority under subsection (1) must be in a form (if any) approved, in writing, by the Secretary.
(2) An authority under subsection (1) may be given subject to conditions specified in the authority.
(3) The Secretary may impose conditions (or further conditions) on the authority given to a person under subsection (1) by giving the person written notice of the conditions.
(4) An authority under subsection (1) may only be given:
(a) to a medical practitioner included in a class of medical practitioners prescribed by the regulations for the purposes of this paragraph; and
(b) to a medical practitioner who has the approval of an ethics committee to supply the specified kinds of medical devices or the specified class of such devices; and
(c) in relation to a class or classes of recipients prescribed by the regulations for the purposes of this paragraph.
However, the regulations may prescribe circumstances in which paragraph (b) does not apply.
(5) The regulations may prescribe circumstances in which medical devices may be supplied under an authority under subsection (1).
(6) The Minister may, by legislative instrument, make rules authorising any health practitioner who is included in a specified class of health practitioners to supply a specified kind of medical device, for use in the treatment of humans, to the class or classes of recipients specified in those rules, so long as:
(a) that kind of medical device is supplied in the circumstances specified in those rules; and
(b) the conditions (if any) specified in those rules are satisfied.
(6A) In making rules under subsection (6), the Minister must comply with:
(a) such requirements (if any) as are prescribed by the regulations; and
(b) such restrictions (if any) as are prescribed by the regulations; and
(c) such limitations (if any) as are prescribed by the regulations.
(6B) If:
(a) a person is authorised, by subsection (6) rules, to supply a specified kind of medical device; and
(b) the person supplies a medical device of that kind in accordance with those rules;
the person must:
(c) notify the supply to the Secretary; and
(d) do so within 28 days after the supply.
(6C) A notification under subsection (6B) must:
(a) be in accordance with a form that is approved, in writing, by the Secretary; and
(b) contain such information as is prescribed by the regulations.
(6D) An approval of a form may require or permit information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
(6E) A person commits an offence if:
(a) the person is subject to a requirement under subsection (6B); and
(b) the person omits to do an act; and
(c) the omission breaches the requirement.
Penalty: 10 penalty units.
(6F) An offence against subsection (6E) is an offence of strict liability.
Note: For strict liability, see section 6.1 of the Criminal Code.
(6FA) Subsection (6E) does not apply in relation to a person and a requirement to notify a supply of a medical device if a health practitioner, on behalf of the person, does the following:
(a) notifies the supply to the Secretary within 28 days after the supply;
(b) makes the notification in accordance with the requirements referred to in subsection (6C).
Note: A defendant bears an evidential burden in relation to the matter in subsection (6FA): see subsection 13.3(3) of the Criminal Code.
(6G) In recommending to the Governor‑General that regulations should be made for the purposes of paragraph (6C)(b), the Minister must have regard to the principle that information should only be prescribed for the purposes of that paragraph if the information is reasonably required for the responsible scrutiny by the Secretary of the operation of the scheme embodied in subsection (6).
(7) In this section:
medical practitioner means a person who is registered, in a State or internal Territory, as a medical practitioner.
41HD Approvals if substitutes for medical devices are unavailable or in short supply
(1) The Secretary may, by notice in writing, grant an approval to a person for:
(a) the importation into Australia of a specified medical device; or
(b) the importation into Australia of a specified medical device and the supply in Australia of that device;
if the Secretary is satisfied that:
(c) the kinds of medical devices included in the Register that could act as a substitute for the medical device are unavailable or are in short supply; and
(d) either:
(i) the medical device is registered or approved for general marketing in at least one foreign country specified in a determination under subsection (5); or
(ii) an application has been made in accordance with section 41FC for inclusion in the Register of the kind of medical device that includes the medical device and the application has passed preliminary assessment; and
(e) the medical device is specified in a determination under subsection (6); and
(f) the approval is necessary in the interests of public health.
Note: For specification by class, see the Acts Interpretation Act 1901 and subsection 13(3) of the Legislation Act 2003.
(1A) The Secretary may, by notice in writing, grant an approval to a person for:
(a) the importation into Australia of a specified medical device; or
(b) the importation into Australia of a specified medical device and the supply in Australia of that device;
if the Secretary is satisfied that:
(c) the kinds of medical devices included in the Register that could act as a substitute for the medical device are unavailable or are in short supply; and
(d) either:
(i) the medical device is not registered or approved for general marketing in any of the foreign countries specified in a determination under subsection (5); or
(ii) the medical device is registered or approved for general marketing in at least one foreign country specified in a determination under subsection (5), but is not readily available for importation into, and supply in, Australia; and
(e) the medical device is registered or approved for general marketing in a foreign country; and
(f) the manufacturing and quality control procedures used in the manufacture of the medical device are acceptable; and
(g) the medical device is specified in a determination under subsection (6); and
(h) the approval is necessary in the interests of public health.
Note: For specification by class, see the Acts Interpretation Act 1901 and subsection 13(3) of the Legislation Act 2003.
(2) The Secretary may, by notice in writing, grant an approval to a person for:
(a) the importation into Australia of a specified medical device; or
(b) the importation into Australia of a specified medical device and the supply in Australia of that device;
if the Secretary is satisfied that:
(c) there are no kinds of medical devices that are included in the Register that could act as a substitute for the medical device; and
(d) an application has been made in accordance with section 41FC for inclusion in the Register of the kind of medical device that includes the medical device and the application has passed preliminary assessment; and
(e) the medical device is specified in a determination under subsection (6); and
(f) the approval is necessary in the interests of public health.
Note: For specification by class, see the Acts Interpretation Act 1901 and subsection 13(3) of the Legislation Act 2003.
Application for approval
(3) An application for an approval must:
(a) be made to the Secretary; and
(b) be accompanied by such information relating to the medical device as is required by the Secretary.
Notification of Secretary’s decision
(4) If an application for an approval is made, the Secretary must, as soon as practicable after deciding the application, notify the applicant of:
(a) the decision; and
(b) if the decision is not to grant the approval—the reasons for the decision.
Determinations
(5) The Secretary may, by legislative instrument, make a determination specifying foreign countries for the purposes of subparagraph (1)(d)(i).
(6) The Secretary may, by legislative instrument, make a determination specifying medical devices that can be the subject of an approval under this section.
Conditions
(7) The Secretary may grant an approval subject to any conditions that are specified in the notice of approval.
Note: Breach of the conditions may be an offence: see subsection 41MN(9).
Period of approval
(8) The Secretary may grant an approval for such period as is specified in the notice of approval.
When approval lapses
(9) The approval lapses if:
(a) the period specified in the notice of approval expires; or
(b) a decision has been made on an application that has been made for inclusion in the Register of the kind of medical device that includes the medical device.
(10) The approval lapses if:
(a) the Secretary is satisfied that paragraph (1)(c), (d), (e) or (f), paragraph (1A)(c), (d), (e), (f), (g) or (h), or paragraph (2)(c), (d), (e) or (f), as the case requires, no longer applies in relation to the medical device, or that a condition of the approval has been contravened; and
(b) the Secretary has given to the person to whom the approval was granted a notice stating that the Secretary is so satisfied.
(11) The lapsing of the approval on the expiry of the period specified in the notice of approval does not prevent another approval being granted under this section in relation to the medical device before that lapsing. The other approval may be expressed to take effect on the expiry of that period.
Approval not a legislative instrument
(12) An approval under subsection (1), (1A) or (2) is not a legislative instrument.
Part 4‑8—Obtaining information
41J What this Part is about
The Secretary may seek information or documents relating to:
• the application of conformity assessment procedures or requirements comparable to those procedures;
• compliance with the essential principles;
• compliance with other requirements;
• distribution of, and other matters relating to, medical devices covered by exemptions under Part 4‑6A or Part 4‑7.
Note: There are additional obligations relating to notifying defects in medical devices: see sections 41MP, 41MPA, 41MQ and 41MR.
Division 1—Information relating to compliance with requirements and other matters
41JA Secretary may require information or documents
(1) The Secretary may, by written notice given to a person:
(a) who is an applicant for a conformity assessment certificate that would relate to a kind of medical device; or
(b) who holds a conformity assessment certificate, or an Australian conformity assessment body certificate, that relates to a kind of medical device; or
(ba) who held, at any time during the notice period under subsection (2), a conformity assessment certificate, or an Australian conformity assessment body certificate, that related to a kind of medical device; or
(c) who is an applicant for the inclusion of a kind of medical device in the Register; or
(d) in relation to whom a kind of medical device is included in the Register; or
(da) in relation to whom a kind of medical device was, at any time during the notice period under subsection (2), included in the Register;
require the person to give to the Secretary information or documents, relating to devices of that kind, that are relevant to one or more of the following:
(e) whether the devices comply with the essential principles;
(f) whether the conformity assessment procedures have been applied to the devices or whether requirements, comparable to those procedures, have been applied to the devices;
(g) whether the devices comply with conditions (if any) imposed on a conformity assessment certificate issued in respect of the device or the inclusion of the device in the Register;
(h) whether either of the following has not been complied with in relation to the devices:
(i) an applicable provision of the Therapeutic Goods Advertising Code;
(ii) any other requirement relating to advertising applicable under Part 5‑1 or under the regulations;
(i) if the kind of medical device is included in the Register in relation to the person—whether medical devices of that kind are being:
(i) supplied in Australia; or
(ii) imported into Australia; or
(iii) exported from Australia;
(ia) the safety and efficacy of the devices for the purposes for which they are to be used;
(ib) the regulatory history of the devices in another country;
(j) any other matter prescribed by the regulations for the purposes of this paragraph.
(1AA) If a notice is given under subsection (1) to a person covered by paragraph (1)(ba), then paragraphs (1)(e) to (j) (to the extent to which they are relevant) apply in relation to the period the person held the certificate.
(1AB) If a notice is given under subsection (1) to a person covered by paragraph (1)(da), then paragraphs (1)(e) to (j) (to the extent to which they are relevant) apply in relation to the period the kind of medical device was included in the Register.
(1A) The Secretary may, by written notice given to a person who is an applicant for a conformity assessment certificate, require the person to give to the Secretary such further information concerning the application as is specified in the notice.
(1B) Requirements under subsections (1) and (1A) may be included in the same notice.
(1C) The Secretary may, by written notice given to a person who holds a conformity assessment certificate, require the person to give to the Secretary specified information to be used by the Secretary in deciding whether to suspend the certificate under section 41EM, or to revoke the certificate under section 41ET, in relation to the circumstances referred to in paragraph 41ET(1)(e).
(1D) Requirements under subsections (1) and (1C) may be included in the same notice.
(1E) The Secretary may, by written notice given to an Australian corporation that has been an Australian conformity assessment body require the corporation to give to the Secretary specified information, or specified documents, relating to:
(a) the certification‑related activities carried on by the corporation while the corporation was an Australian conformity assessment body; or
(b) the conditions referred to in subsection 41EWA(5) that applied while the corporation was an Australian conformity assessment body.
(2) For the purposes of paragraphs (1)(ba) and (da), the notice period is the period:
(a) of the length specified in the regulations; and
(b) ending on the day before the Secretary gives the notice under subsection (1).
(3) Nothing in this section affects the operation of Part VIIC of the Crimes Act 1914 (which includes provisions that, in certain circumstances, relieve persons from the requirement to disclose spent convictions and require persons aware of such convictions to disregard them).
41JB Complying with the Secretary’s requirements
(1) The person must give the information or documents to the Secretary:
(a) within such reasonable time, being not less than 10 working days from the day on which the notice is given, as is specified in the notice; and
(b) in such form as is specified in the notice.
(2) The form may require or permit information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
Offence for failing to comply with a notice
(3) A person commits an offence if:
(a) the person is given a notice under section 41JA; and
(aa) the person is covered by paragraph 41JA(1)(b), (ba), (d) or (da) or subsection 41JA(1E); and
(b) the person fails to comply with the notice.
Penalty: 500 penalty units.
Note: Failure to comply with the notice might also lead to suspension or revocation of a conformity assessment certificate (see Divisions 3 and 4 of Part 4‑4) or suspension or cancellation of the entry of a kind of medical device in the Register (see Part 4‑6).
(3A) Subsection (3) does not apply if the person has a reasonable excuse.
Note: A defendant bears an evidential burden in relation to the matter in subsection (3A): see subsection 13.3(3) of the Criminal Code.
(3B) A person commits an offence if:
(a) the person is given a notice under section 41JA; and
(b) the person is covered by paragraph 41JA(1)(b), (ba), (d) or (da) or subsection 41JA(1E); and
(d) the person fails to comply with the notice.
Penalty: 100 penalty units.
(3C) An offence against subsection (3B) is an offence of strict liability.
(3D) Subsection (3B) does not apply if the person has a reasonable excuse.
Note: A defendant bears an evidential burden in relation to the matter in subsection (3D): see subsection 13.3(3) of the Criminal Code.
Offences for giving false or misleading information in purported compliance with a notice
(4) A person commits an offence if:
(a) the person is given a notice under section 41JA in relation to a kind of medical device; and
(b) the person gives information in purported compliance with the notice; and
(c) the information is false or misleading in a material particular; and
(d) either:
(i) the use of the kind of medical device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the kind of medical device, if the kind of medical device were used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (7) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(7) A person commits an offence if:
(a) the person is given a notice under section 41JA; and
(b) the person gives information in purported compliance with the notice; and
(c) the information is false or misleading in a material particular.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(8) A person commits an offence if:
(a) the person is given a notice under section 41JA; and
(b) the person gives information in purported compliance with the notice; and
(c) the information is false or misleading in a material particular.
Penalty: 100 penalty units.
(9) An offence against subsection (8) is an offence of strict liability.
41JBA Civil penalty for giving false or misleading information in purported compliance with a notice
A person contravenes this section if:
(a) the person is given a notice under section 41JA; and
(b) the person gives information in purported compliance with the notice; and
(c) the information is false or misleading in a material particular.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
41JC Self‑incrimination
(1) A person is not excused from giving information or a document under section 41JB on the ground that to do so would tend to incriminate the person or expose the person to a penalty.
(2) However, in the case of an individual:
(a) the information given; or
(b) the giving of the document; or
(c) any information, document or thing obtained as a direct or indirect consequence of giving the information or document;
is not admissible in evidence in:
(d) criminal proceedings against the individual, except proceedings under, or arising out of, subsection 41JB(4), (7) or (8); or
(e) proceedings for a pecuniary penalty order against the individual for a contravention of a civil penalty provision, except civil proceedings under, or arising out of, section 41JBA.
Division 2—Information relating to medical devices covered by exemptions
41JCA Secretary may require information etc. about medical devices exempt under Part 4‑6A
(1) This section applies to a person who is required to comply with a condition of an exemption of a kind of medical device under section 41GS.
(2) The Secretary may, by written notice given to the person, require the person to give to the Secretary specified information or documents relating to one or more of the following:
(a) the supply of devices of that kind;
(b) the handling of devices of that kind;
(c) the monitoring of the supply of devices of that kind;
(d) the results of the supply of devices of that kind;
(e) any other matter prescribed by the regulations for the purposes of this paragraph in relation to devices of that kind.
(3) The notice must specify a reasonable period within which the person to whom the notice is given must comply. The period must be at least 10 working days starting on the day on which the notice is given.
(4) The notice may require information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
41JD Secretary may require information etc. about devices exempted under section 41HA from inclusion in the Register
(1) The Secretary may give the sponsor of kinds of medical devices exempted under subsection 41HA(1) from Division 3 of Part 4‑11, a written notice requiring the sponsor to give to the Secretary specified information or documents relating to one or more of the following:
(a) the supply of devices of those kinds;
(b) the handling of devices of those kinds;
(c) the monitoring of the supply of devices of those kinds;
(d) the results of the supply of devices of those kinds;
(e) any other matter prescribed by the regulations for the purposes of this paragraph in relation to devices of those kinds.
(2) If a medical device is exempt under subsection 41HA(1) because a medical practitioner has signed a statement in accordance with regulations made for the purposes of this section, the Secretary may give the medical practitioner a written notice requiring the medical practitioner to give to the Secretary specified information or documents relating to one or more of the following:
(a) the condition of the person to whom the medical device is to be given or is given;
(b) the supply of the device;
(c) the handling of the device;
(d) the monitoring of the supply of the device;
(e) the results of the supply of the device;
(f) any other matter prescribed by the regulations for the purposes of this paragraph in relation to medical devices of that kind.
(3) A notice under this section must specify a reasonable period within which the person must comply. The period must be at least 10 working days starting on the day on which the notice is given.
(4) A notice under this section may require information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
41JE Secretary may require information relating to approvals under section 41HB
Approval under subsection 41HB(1)
(1) The Secretary may give to a person granted an approval under subsection 41HB(1) (special and experimental uses), in relation to specified kinds of medical devices, a written notice requiring the person to give to the Secretary specified information or documents relating to one or more of the following:
(a) the supply of devices of those kinds;
(b) the handling of devices of those kinds;
(c) the monitoring of the supply of devices of those kinds;
(d) the results of the supply of devices of those kinds;
(e) any other matter prescribed by the regulations for the purposes of this paragraph in relation to devices of those kinds.
Approval under subsection 41HB(1)—use by another person
(2) The Secretary may give to a person using specified kinds of medical devices, that are the subject of an approval granted to someone else under paragraph 41HB(1)(e) (use solely for experimental purposes in humans), a written notice requiring the person to give to the Secretary specified information or documents relating to either of both of the following:
(a) the use of devices of those kinds;
(b) any other matter prescribed by the regulations for the purposes of this paragraph in relation to devices of those kinds.
Compliance period
(3) A notice under this section must specify a reasonable period within which the person to whom the notice is given must comply. The period must be at least 10 working days starting on the day on which the notice is given.
Information may need to be given in accordance with specified software requirements
(4) A notice under this section may require information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
41JF Secretary may require information relating to health practitioner authorisations
(1) The Secretary may give to a person who is granted an authority under subsection 41HC(1) (exemptions for medical practitioners), in relation to specified kinds of medical devices, a written notice requiring the person to give to the Secretary specified information or documents relating to one or more of the following:
(a) the supply of devices of those kinds;
(b) the handling of devices of those kinds;
(c) the monitoring of the supply of devices of those kinds;
(d) the results of the supply of devices of those kinds;
(e) any other matter prescribed by the regulations for the purposes of this paragraph in relation to devices of those kinds.
(1A) If a person is authorised, by subsection 41HC(6) rules, to supply a specified kind of medical device, the Secretary may give the person a written notice requiring the person to give the Secretary specified information or documents relating to one or more of the following:
(a) the supply of devices of that kind;
(b) the handling of devices of that kind;
(c) the monitoring of the supply of devices of that kind;
(d) the results of the supply of devices of that kind;
(e) any other matter prescribed by the regulations for the purposes of this paragraph in relation to devices of that kind.
(2) A notice under subsection (1) or (1A) must specify a reasonable period within which the person to whom the notice is given must comply. The period must be at least 10 working days starting on the day on which the notice is given.
(3) A notice under subsection (1) or (1A) may require information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
41JFA Secretary may require information relating to approvals under section 41HD
(1) The Secretary may give to a person who is granted an approval under subsection 41HD(1), (1A) or (2) in relation to a medical device a written notice requiring the person to give to the Secretary specified information or documents relating to one or more of the following:
(a) the supply of the medical device;
(b) the handling of the medical device;
(c) the monitoring of the supply of the medical device;
(d) the results of the supply of the medical device;
(e) any other matter prescribed by the regulations for the purposes of this paragraph in relation to the kind of medical device that includes the medical device.
(2) The notice must specify a reasonable period within which the person must comply. The period must be at least 10 working days starting on the day on which the notice is given.
(3) The notice may require information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
41JG Criminal offences for failing to give information or documents sought under this Division
(1) A person commits an offence if:
(a) the person is given a notice under section 41JCA, 41JD, 41JE, 41JF or 41JFA; and
(b) the person fails to comply with the notice.
Penalty: 400 penalty units.
(2) A person commits an offence if:
(a) the person is given a notice under section 41JCA, 41JD, 41JE, 41JF or 41JFA; and
(b) the person fails to comply with the notice.
Penalty: 100 penalty units.
(3) An offence against subsection (2) is an offence of strict liability.
41JH False or misleading information
(1) A person to whom a notice is given under section 41JCA, 41JD, 41JE, 41JF or 41JFA commits an offence if:
(a) the person gives information to the Secretary; and
(b) the person knows that the information:
(i) is false or misleading; or
(ii) omits any matter or thing without which the information is misleading; and
(c) the information is given in compliance or purported compliance with the notice.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) A person to whom a notice is given under section 41JCA, 41JD, 41JE, 41JF or 41JFA commits an offence if:
(a) the person gives information to the Secretary; and
(b) the information:
(i) is false or misleading; or
(ii) omits any matter or thing without which the information is misleading; and
(c) the information is given in compliance or purported compliance with the notice.
Penalty: 100 penalty units.
(3) An offence against subsection (2) is an offence of strict liability.
(4) Subsection (1) or (2) does not apply as a result of subparagraph (1)(b)(i) or (2)(b)(i) if the information is not false or misleading in a material particular.
Note: A defendant bears an evidential burden in relation to the matter in subsection (4): see subsection 13.3(3) of the Criminal Code.
(5) Subsection (1) or (2) does not apply as a result of subparagraph (1)(b)(ii) or (2)(b)(ii) if the information did not omit any matter or thing without which the information is misleading in a material particular.
Note: A defendant bears an evidential burden in relation to the matter in subsection (5): see subsection 13.3(3) of the Criminal Code.
41JI False or misleading documents
(1) A person commits an offence if:
(a) the person produces a document to the Secretary; and
(b) the person knows that the document is false or misleading; and
(c) the document is produced in compliance or purported compliance with a notice given under section 41JCA, 41JD, 41JE, 41JF or 41JFA.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(1A) A person commits an offence if:
(a) the person produces a document to the Secretary; and
(b) the document is false or misleading; and
(c) the document is produced in compliance or purported compliance with a notice given under section 41JCA, 41JD, 41JE, 41JF or 41JFA.
Penalty: 100 penalty units.
(1B) An offence against subsection (1A) is an offence of strict liability.
(1C) Subsection (1) or (1A) does not apply if the document is not false or misleading in a material particular.
Note: A defendant bears an evidential burden in relation to the matter in subsection (1C): see subsection 13.3(3) of the Criminal Code.
(2) Subsection (1) or (1A) does not apply to a person who produces a document if the document is accompanied by a written statement signed by the person or, in the case of a body corporate, by a competent officer of the body corporate:
(a) stating that the document is, to the knowledge of the first‑mentioned person, false or misleading in a material particular; and
(b) setting out, or referring to, the material particular in which the document is, to the knowledge of the first‑mentioned person, false or misleading.
Note: A defendant bears an evidential burden in relation to the matter in subsection (2) (see subsection 13.3(3) of the Criminal Code).
41JJ Self‑incrimination
(1) A person is not excused from giving information or a document under a notice given under section 41JCA, 41JD, 41JE, 41JF or 41JFA on the ground that to do so would tend to incriminate the person or expose the person to a penalty.
(2) However, in the case of an individual:
(a) the information given; or
(b) the giving of the document; or
(c) any information, document or thing obtained as a direct or indirect consequence of giving the information or document;
is not admissible in evidence in:
(d) criminal proceedings against the individual, except proceedings under, or arising out of, section 41JH or 41JI; or
(e) proceedings for a pecuniary penalty order against the individual for a contravention of a civil penalty provision.
Part 4‑9—Public notification, and recall, of medical devices
41K What this Part is about
The Secretary can require action to recall medical devices, or to inform the public about medical devices, that do not comply with requirements or cannot lawfully be supplied.
41KA Public notification, and recall, of medical devices
(1) The Secretary may, in writing, impose requirements, relating to a kind of medical device, on a person if:
(a) any of the circumstances referred to in the second column of an item in the following table occur in relation to the kind of device; and
(b) the person is referred to in the third column of that item of the table.
Circumstances in which requirements may be imposed |
Item | Circumstance relating to a kind of medical device | Person subject to requirements |
1. | It is supplied while it is included in the Register, but the Secretary is satisfied that medical devices of that kind do not comply with the essential principles | The person in relation to whom it is included in the Register |
2. | It is supplied while it is included in the Register, but the Secretary is satisfied that the conformity assessment procedures have not been applied to medical devices of that kind and that requirements, comparable to those procedures, have not been applied to medical devices of that kind | The person in relation to whom it is included in the Register |
3. | It is supplied while: (a) medical devices of that kind are exempt devices; or (b) there is an approval under section 41HB relating to devices of that kind; or (c) there is an authority under section 41HC relating to devices of that kind; or (d) there is an approval under subsection 41HD(1), (1A) or (2) relating to devices of that kind; but the Secretary is satisfied that medical devices of that kind do not comply with the essential principles | The person supplying the kind of medical device |
4. | It is supplied while: (a) medical devices of that kind are exempt devices; or (b) there is an approval under section 41HB relating to devices of that kind; or (c) there is an authority under section 41HC relating to devices of that kind; or (d) there is an approval under subsection 41HD(1), (1A) or (2) relating to devices of that kind; but the Secretary is satisfied that the conformity assessment procedures have not been applied to medical devices of that kind and that requirements, comparable to those procedures, have not been applied to medical devices of that kind | The person supplying the kind of medical device |
5. | It is supplied while: (a) it is not included in the Register; and (aa) it is not covered by an exemption in force under section 41GS; and (b) it is not an exempt device; and (c) there is not an approval under section 41HB relating to devices of that kind; and (d) there is not an authority under section 41HC relating to devices of that kind; and (e) there is not an approval under subsection 41HD(1), (1A) or (2) relating to devices of that kind. | The person supplying the kind of medical device |
5A. | It is supplied while it is covered by an exemption in force under section 41GS, and the Secretary is satisfied that it is not fit to be used for its intended purpose | The person supplying the kind of medical device |
5B. | It is supplied while it is included in the Register, but it appears to the Secretary that the quality, safety or performance of medical devices of that kind is unacceptable | The person in relation to whom the kind of medical device is included in the Register |
6. | It has been suspended from the Register | The person in relation to whom it was included in the Register |
7. | Its entry has been cancelled from the Register | The person in relation to whom it was included in the Register |
8. | It is counterfeit goods (within the meaning of section 42E) | The person supplying the kind of medical device |
(2) The requirements may be one or more of the following:
(a) to take specified steps, in the specified manner and within such reasonable period as is specified, to recall medical devices of that kind that have been distributed;
(b) to inform the public or a specified class of persons, in the specified manner and within such reasonable period as is specified, to the effect that the circumstances referred to in paragraph (1)(a) have occurred in relation to medical devices of that kind;
(c) to inform the public or a specified class of persons, in the specified manner and within such reasonable period as is specified, of specified information, or of information of a specified kind, relating to either or both of the following:
(i) medical devices of that kind;
(ii) the circumstances referred to in paragraph (1)(a);
(d) to publish, in the specified manner and within such reasonable period as is specified, specified information, or information of a specified kind, relating to the manufacture or distribution of medical devices of that kind;
(e) to notify the Secretary, in the specified manner and within such reasonable period as is specified, of specified information, or of information of a specified kind, relating to the persons to whom medical devices of that kind have been supplied.
(3) If the circumstances referred to in paragraph (1)(a) apply only to some medical devices of that kind, the Secretary may limit the imposition of the requirements to the medical devices of that kind to which those circumstances apply.
(4) A requirement to recall medical devices under this section does not apply to a medical device that cannot be recalled because it has been administered to, or applied in the treatment of, a person.
41KB Publication of requirements
The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after imposing a requirement under section 41KA, a notice setting out particulars of the requirement.
41KC Criminal offences for failing to comply with requirements relating to a kind of medical device
(1) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a requirement imposed on the person under section 41KA; and
(c) the act or omission has resulted in, will result in, or is likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a requirement imposed on the person under section 41KA.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(5) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a requirement imposed on the person under section 41KA.
Penalty: 100 penalty units.
(6) An offence against subsection (5) is an offence of strict liability.
41KCA Civil penalty for failing to comply with requirements relating to a kind of medical device
A person contravenes this section if:
(a) the person does an act or omits to do an act; and
(b) the act or omission contravenes a requirement imposed on the person under section 41KA.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
41KD Powers of suspension and cancellation unaffected
Imposition of a requirement under section 41KA does not affect the Secretary’s powers to:
(a) suspend the entry of a kind of medical device, or some medical devices of a particular kind, from the Register under Part 4‑6; or
(b) cancel the entry of a kind of medical device, or some medical devices of a particular kind, in the Register under Part 4‑6.
41KE Saving of other laws
This Part is not intended to exclude or limit the operation of any other law of the Commonwealth or any law of a State or Territory.
Part 4‑10—Assessment fees
41L What this Part is about
Conformity assessment fees must be paid for consideration of applications for conformity assessment certificates. Application audit assessment fees must be paid for auditing applications that are required to be selected for auditing under paragraph 41FH(1)(a).
41LA Assessment fees
(1) A conformity assessment fee specified in or determined in accordance with the regulations is payable by a person in respect of consideration of an application for a conformity assessment certificate under Part 4‑4.
(2) The regulations may prescribe different levels of conformity assessment fees in relation to any one or more of the following:
(a) different kinds of manufacturers;
(b) different kinds of medical devices;
(c) different parts of the conformity assessment procedures that are considered in relation to an application for a conformity assessment certificate under Part 4‑4.
(3) An application audit assessment fee specified in or determined in accordance with the regulations is payable by a person in respect of the auditing of an application for inclusion of a kind of medical device in the Register under Part 4‑5, if paragraph 41FH(1)(a) required the Secretary to select the application for audit.
(4) The regulations may prescribe different levels of application audit assessment fees in relation to any one or more of the following:
(a) different kinds of manufacturers;
(b) different kinds of medical devices;
(c) different levels of assessment of kinds of medical devices.
(5) The application audit assessment fee payable because of subsection (3) is payable only in respect of considering the matters set out in subsection 41FI(1).
41LB When assessment fee due for payment
Subject to sections 41LC and 41LE, an assessment fee payable by an applicant is due and payable on the day, and in the manner, specified in the regulations.
41LC Payment of assessment fee by instalments
(1) The regulations may provide for the payment of an assessment fee to be made by such instalments and at such times as are ascertained in accordance with the regulations, and the assessment fee is due and payable accordingly.
(2) Regulations made for the purposes of subsection (1) may provide that a person is not allowed to pay an assessment fee by instalments if any part of an instalment of:
(a) that or any other assessment fee payable by the person; or
(b) any evaluation fee under section 24 payable by the person;
was unpaid immediately after the time when it became due for payment.
(3) Subsection (2) does not limit the generality of subsection (1).
41LD Recovery of assessment fee
An assessment fee may be recovered by the Commonwealth as a debt due to the Commonwealth.
41LE Reduction of conformity assessment fee where decision not made within prescribed period
(1) Nothing in section 41LA, 41LB or 41LC requires the applicant to pay more than 3/4 of the conformity assessment fee before the making of the decision if:
(a) the application is for the issuing of a conformity assessment certificate under Part 4‑4; and
(b) consideration of the application will involve an examination of the design of medical devices; and
(c) a period is prescribed under paragraph 63(2)(dc) for making a decision on the application.
(2) If the decision is not made within that period, the conformity assessment fee is 3/4 of the fee that, apart from this subsection, would have been the conformity assessment fee.
(3) If:
(a) the decision is made within that period; and
(b) part of the conformity assessment fee under section 41LA is, because of subsection (1) of this section, unpaid when the decision is made;
that part becomes due and payable on the making of the decision.
(4) For the purposes of this section, a decision is taken to be made on the application when the applicant is notified under subsection 41EE(1) of the Secretary’s decision on the application.
Part 4‑11—Offences and civil penalty provisions relating to medical devices
41M What this Part is about
This Part contains offences and civil penalty provisions that are aimed at ensuring that:
• the essential principles are complied with (see Division 1);
• the conformity assessment procedures have been applied to kinds of medical devices or requirements, comparable to those procedures, have been applied to kinds of medical devices (see Division 2);
• administrative processes put in place by Parts 4‑4 to 4‑9 are followed (see Divisions 3, 3A and 4).
Note: There are also some offences and civil penalty provisions in the earlier Parts of this Chapter. They generally relate to matters ancillary to administrative processes in those Parts (e.g. false or misleading statements in applications).
Division 1—Non‑compliance with essential principles
41MA Criminal offences for importing, supplying or exporting a medical device that does not comply with essential principles
Offences relating to importing a medical device
(1) A person commits an offence if:
(a) the person imports a medical device into Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device; and
(c) the Secretary has not consented to the importation; and
(ca) the device is not of a kind covered by an exemption in force under section 41GS; and
(d) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the device does not comply with the essential principles.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person imports a medical device into Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device; and
(c) the Secretary has not consented to the importation; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(4A) A person commits an offence if:
(a) the person imports a medical device into Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device; and
(c) the Secretary has not consented to the importation; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: 100 penalty units.
(4B) An offence against subsection (4A) is an offence of strict liability.
Offences relating to supplying a medical device
(5) A person commits an offence if:
(a) the person supplies a medical device for use in Australia; and
(b) the medical device does not comply with the essential principles; and
(c) the Secretary has not consented to the supply; and
(ca) the device is not of a kind covered by an exemption in force under section 41GS; and
(d) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if device were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the device does not comply with the essential principles.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (8) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(8) A person commits an offence if:
(a) the person supplies a medical device for use in Australia; and
(b) the medical device does not comply with the essential principles; and
(c) the Secretary has not consented to the supply; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(8A) A person commits an offence if:
(a) the person supplies a medical device for use in Australia; and
(b) the medical device does not comply with the essential principles; and
(c) the Secretary has not consented to the supply; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: 100 penalty units.
(8B) An offence against subsection (8A) is an offence of strict liability.
Offences relating to exporting a medical device
(9) A person commits an offence if:
(a) the person exports a medical device from Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device for supply in Australia; and
(c) the Secretary has not consented to the exportation; and
(ca) the device is not of a kind covered by an exemption in force under section 41GS; and
(d) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the device does not comply with the essential principles.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (12) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(12) A person commits an offence if:
(a) the person exports a medical device from Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device for supply in Australia; and
(c) the Secretary has not consented to the exportation; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(13) A person commits an offence if:
(a) the person exports a medical device from Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device for supply in Australia; and
(c) the Secretary has not consented to the exportation; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: 100 penalty units.
(14) An offence against subsection (13) is an offence of strict liability.
41MAA Civil penalties for importing, supplying or exporting a medical device that does not comply with essential principles
Civil penalty relating to importing a medical device
(1) A person contravenes this subsection if:
(a) the person imports a medical device into Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device; and
(c) the Secretary has not consented to the importation; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Civil penalty relating to supplying a medical device
(2) A person contravenes this subsection if:
(a) the person supplies a medical device for use in Australia; and
(b) the medical device does not comply with the essential principles; and
(c) the Secretary has not consented to the supply; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Civil penalty relating to exporting a medical device
(3) A person contravenes this subsection if:
(a) the person exports a medical device from Australia; and
(b) the medical device does not comply with the essential principles relating to matters other than the labelling of the device for supply in Australia; and
(c) the Secretary has not consented to the exportation; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
41MB Exceptions
(1) Sections 41MA and 41MAA do not apply if:
(a) the medical device complies with one or more medical device standards that apply to it; and
(b) the medical device fails to comply with the essential principles only in respect of a part or parts of the essential principles to which that medical device standard, or one or more of those medical device standards, relate.
Note: Medical device standards are determined under Division 2 of Part 4‑2.
(2) For the purposes of this section, a medical device standard relates to a part or parts of the essential principles only if the standard specifies that part or parts.
Note 1: In the prosecution for an offence, the defendant bears an evidential burden in relation to the matters in this section (see subsection 13.3(3) of the Criminal Code).
Note 2: In proceedings for the contravention of a civil penalty provision, the defendant must prove the matters in this section.
41MC Criminal offences relating to breaching a condition of a consent
(1) The consent of the Secretary under section 41MA or 41MAA may be given:
(a) unconditionally or subject to conditions; or
(b) in respect of particular medical devices or kinds of medical devices.
(2) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a condition of a consent; and
(c) the act or omission has resulted in, will result in, or is likely to result in, harm or injury to any person.
Penalty: 2,000 penalty units.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (5) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(5) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a condition of a consent.
Penalty: 500 penalty units.
(6) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a condition of a consent.
Penalty: 100 penalty units.
(7) An offence against subsection (6) is an offence of strict liability.
41MCA Civil penalty relating to breaching a condition of a consent
A person contravenes this section if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches a condition of a consent imposed under section 41MC.
Maximum civil penalty:
(a) for an individual—3,000 penalty units; and
(b) for a body corporate—30,000 penalty units.
41MD Treating medical devices as prohibited imports or exports
If:
(a) the importation or exportation of a medical device is an offence under subsection 41MA(1), (4), (4A), (9), (12) or (13) or a contravention of subsection 41MAA(1) or (3); and
(b) the Secretary notifies the Comptroller‑General of Customs in writing that the Secretary wishes the Customs Act 1901 to apply to that importation or exportation;
the Customs Act 1901 has effect as if the device included in that importation or exportation were goods described as forfeited to the Crown under section 229 of that Act because they were:
(c) prohibited imports within the meaning of that Act; or
(d) prohibited exports within the meaning of that Act;
as the case requires.
Division 2—Failure to apply conformity assessment procedures
41ME Criminal offences for failing to apply conformity assessment procedures—manufacturers
Offences relating to supplying a medical device
(1) A person commits an offence if:
(a) the person manufactures a medical device; and
(b) the person supplies the device in Australia; and
(c) the conformity assessment procedures have not been applied to the device; and
(ca) the device is not of a kind covered by an exemption in force under section 41GS; and
(d) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the conformity assessment procedures have not been applied to the device.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person manufactures a medical device; and
(b) the person supplies the device in Australia; and
(c) the conformity assessment procedures have not been applied to the device; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(4A) A person commits an offence if:
(a) the person manufactures a medical device; and
(b) the person supplies the device in Australia; and
(c) the conformity assessment procedures have not been applied to the device; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: 100 penalty units.
(4B) An offence against subsection (4A) is an offence of strict liability.
Offences relating to exporting a medical device
(5) A person commits an offence if:
(a) the person manufactures a medical device; and
(b) the person exports the device from Australia; and
(c) the conformity assessment procedures have not been applied to the device; and
(ca) the device is not of a kind covered by an exemption in force under section 41GS; and
(d) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the conformity assessment procedures have not been applied to the device.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (8) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(8) A person commits an offence if:
(a) the person manufactures a medical device; and
(b) the person exports the device from Australia; and
(c) the conformity assessment procedures have not been applied to the device; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(9) A person commits an offence if:
(a) the person manufactures a medical device; and
(b) the person exports the device from Australia; and
(c) the conformity assessment procedures have not been applied to the device; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: 100 penalty units.
(10) An offence against subsection (9) is an offence of strict liability.
41MEA Civil penalties for failing to apply conformity assessment procedures—manufacturers
Civil penalty relating to supplying a medical device
(1) A person contravenes this subsection if:
(a) the person supplies a medical device in Australia; and
(b) the person has manufactured the device; and
(c) the conformity assessment procedures have not been applied to the device; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Civil penalty relating to exporting a medical device
(2) A person contravenes this subsection if:
(a) the person exports a medical device from Australia; and
(b) the person has manufactured the device; and
(c) the conformity assessment procedures have not been applied to the device; and
(d) the device is not of a kind covered by an exemption in force under section 41GS.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
41MF Criminal offences for failing to apply conformity assessment procedures—sponsors
Offences relating to supplying a medical device
(1) A person commits an offence if:
(a) the person supplies a medical device in Australia; and
(b) the conformity assessment procedures have not been applied to the device; and
(ba) the device is not of a kind covered by an exemption in force under section 41GS; and
(c) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(d) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the conformity assessment procedures have not been applied to the device.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (2) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) A person commits an offence if:
(a) the person supplies a medical device in Australia; and
(b) the conformity assessment procedures have not been applied to the device; and
(c) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Offences relating to exporting a medical device
(3) A person commits an offence if:
(a) the person exports a medical device from Australia; and
(b) the conformity assessment procedures have not been applied to the device; and
(ba) the device is not of a kind covered by an exemption in force under section 41GS; and
(c) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(d) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the conformity assessment procedures have not been applied to the device.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person exports a medical device from Australia; and
(b) the conformity assessment procedures have not been applied to the device; and
(c) the device is not of a kind covered by an exemption in force under section 41GS.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Exception
(5) This section does not apply if the defendant was not the sponsor of the device at the time of the supply or exportation, as the case may be.
Note: A defendant bears an evidential burden in relation to the matters in subsection (5): see subsection 13.3(3) of the Criminal Code.
41MG Exceptions
(1) Sections 41ME, 41MEA and 41MF do not apply to the extent that:
(a) the quality management systems applied to the medical device comply with one or more conformity assessment standards that apply to them; and
(b) the conformity assessment procedures have not been applied to the device only in respect of a part or parts of the conformity assessment procedures to which one or more of those conformity assessment standards relate.
Note: Conformity assessment standards are determined under Division 2 of Part 4‑3.
(2) For the purposes of this section, a conformity assessment standard relates to a part or parts of the conformity assessment procedures only if the standard specifies that part or parts.
(3) Sections 41ME, 41MEA and 41MF do not apply if an overseas regulator conformity assessment document is in force in relation to the medical device.
Note 1: In the prosecution for an offence, the defendant bears an evidential burden in relation to the matters in this section (see subsection 13.3(3) of the Criminal Code).
Note 2: In proceedings for the contravention of a civil penalty provision, the defendant must prove the matters in this section.
41MH Criminal offence for making false statements in declarations
A person commits an offence if:
(a) the person makes a statement in or in connection with a declaration, relating to the application of conformity assessment procedures, or the application of requirements comparable to those procedures, to a medical device that the person has manufactured; and
(b) the statement is false or misleading in a material particular.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
41MHA Civil penalty for making false statements in declarations
A person contravenes this section if:
(a) the person manufactures a medical device; and
(b) the person makes a statement in or in connection with a declaration relating to the application of conformity assessment procedures, or the application of requirements comparable to those procedures, to the device; and
(c) the statement is false or misleading in a material particular.
Maximum civil penalty:
(a) for an individual—3,000 penalty units; and
(b) for a body corporate—30,000 penalty units.
Division 3—Medical devices not included in the Register and related matters
41MI Criminal offences for importing, exporting, supplying or manufacturing a medical device not included in the Register
(1) A person commits an offence if:
(a) the person:
(i) imports a medical device into Australia; or
(ii) exports a medical device from Australia; or
(iii) supplies a medical device in Australia; or
(iv) manufactures a medical device in Australia; and
(b) none of the following subparagraphs applies in relation to the device:
(i) the device is of a kind included in the Register in relation to the person;
(ia) the device is of a kind covered by an exemption in force under section 41GS;
(ii) the device is an exempt device;
(iii) the device is the subject of an approval under section 41HB or an authority under section 41HC;
(iv) the device is the subject of an approval under subsection 41HD(1), (1A) or (2) that is held by the person; and
(c) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person:
(i) imports a medical device into Australia; or
(ii) exports a medical device from Australia; or
(iii) supplies a medical device in Australia; or
(iv) manufactures a medical device in Australia; and
(b) none of the following subparagraphs applies in relation to the device:
(i) the device is of a kind included in the Register in relation to the person;
(ia) the device is of a kind covered by an exemption in force under section 41GS;
(ii) the device is an exempt device;
(iii) the device is the subject of an approval under section 41HB or an authority under section 41HC;
(iv) the device is the subject of an approval under subsection 41HD(1), (1A) or (2) that is held by the person.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(5) A person commits an offence if:
(a) the person:
(i) imports a medical device into Australia; or
(ii) exports a medical device from Australia; or
(iii) supplies a medical device in Australia; or
(iv) manufactures a medical device in Australia; and
(b) none of the following subparagraphs applies in relation to the device:
(i) the device is of a kind included in the Register in relation to the person;
(ii) the device is of a kind covered by an exemption in force under section 41GS;
(iii) the device is an exempt device;
(iv) the device is the subject of an approval under section 41HB or an authority under section 41HC;
(v) the device is the subject of an approval under subsection 41HD(1), (1A) or (2) that is held by the person.
Penalty: 100 penalty units.
(5A) An offence against subsection (5) is an offence of strict liability.
Defence if person was not the sponsor of the goods
(6) It is a defence to a prosecution under subsection (1), (4) or (5) if the defendant proves that the defendant was not the sponsor of the device at the time of the importation, exportation, supply, or manufacture, as the case may be.
Note: A defendant bears a legal burden in relation to the matters in subsection (6): see section 13.4 of the Criminal Code.
Exception
(7) Subsection (1) does not apply if:
(a) harm or injury did not, will not, or is not likely to, directly result from:
(i) the quality, safety or performance of the medical device; or
(ii) a matter relating to the labelling or packaging of the medical device; or
(iii) the improper use of the medical device; or
(b) harm or injury would not, or would not be likely to, directly result from:
(i) the quality, safety or performance of the medical device; or
(ii) a matter relating to the labelling or packaging of the medical device; or
(iii) the improper use of the medical device.
Note: A defendant bears an evidential burden in relation to the matters in subsection (7): see subsection 13.3(3) of the Criminal Code.
41MIA Notice required to adduce evidence in support of exception under subsection 41MI(7)
(1) If:
(a) a defendant is committed for trial for an offence against subsection 41MI(1); or
(b) an offence against subsection 41MI(1) is to be heard and determined by a court of summary jurisdiction;
the committing magistrate or the court must:
(c) inform the defendant of the requirements of this section; and
(d) cause a copy of this section to be given to the defendant.
(2) A defendant must not, without leave of the court, adduce evidence in support of the exception under subsection 41MI(7) unless:
(a) if paragraph (1)(a) applies—more than 21 days before the trial begins; or
(b) if paragraph (1)(b) applies—more than 21 days before the hearing of the offence begins;
he or she gives notice of particulars of the exception.
(3) A defendant must not, without leave of the court, call any other person to give evidence in support of the exception unless:
(a) the notice under subsection (2) includes the name and address of the person or, if the name and address is not known to the defendant at the time he or she gives the notice, any information in his or her possession that might be of material assistance in finding the person; and
(b) if the name or the address is not included in the notice—the court is satisfied that the defendant before giving the notice took, and after giving the notice continued to take, all reasonable steps to ascertain the name or address; and
(c) if the name or address is not included in the notice, but the defendant subsequently ascertains the name or address or receives information that might be of material assistance in finding the person—the defendant immediately gives notice of the name, address or other information, as the case may be; and
(d) if the defendant is told by or on behalf of the prosecutor that the person has not been found by the name, or at the address, given by the defendant:
(i) the defendant immediately gives notice of any information in the defendant’s possession that might be of material assistance in finding the person; or
(ii) if the defendant later receives any such information—the defendant immediately gives notice of the information.
(4) A notice purporting to be given under this section on behalf of the defendant by his or her legal practitioner is, unless the contrary is proved, taken as having been given with the authority of the defendant.
(5) Any evidence tendered to disprove that the exception applies may, subject to direction by the court, be given before or after evidence is given in support of the exception.
(6) A notice of particulars of the exception must be given, in writing, to the Director of Public Prosecutions. A notice is taken as having been given if it is:
(a) delivered to or left at the Office of the Director of Public Prosecutions; or
(b) sent by certified mail addressed to the Director of Public Prosecutions at the Office of the Director of Public Prosecutions.
(7) In this section:
Director of Public Prosecutions means a person holding office as, or acting as, the Director of Public Prosecutions under the Director of Public Prosecutions Act 1983.
41MIB Civil penalty for importing, exporting, supplying or manufacturing a medical device not included in the Register
(1) A person contravenes this section if:
(a) the person does any of the following:
(i) imports a medical device into Australia;
(ii) exports a medical device from Australia;
(iii) supplies a medical device in Australia;
(iv) manufactures a medical device in Australia; and
(b) none of the following subparagraphs apply in relation to the device:
(i) the device is of a kind included in the Register in relation to the person;
(ia) the device is of a kind covered by an exemption in force under section 41GS;
(ii) the device is an exempt device;
(iii) the device is the subject of an approval under section 41HB or an authority under section 41HC;
(iv) the device is the subject of an approval under subsection 41HD(1), (1A) or (2) that is held by the person.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Exception
(2) Subsection (1) does not apply if the defendant proves that the defendant was not the sponsor of the device at the time of the importation, exportation, supply, or manufacture, as the case may be.
41MJ Treating medical devices as prohibited imports or exports
If:
(a) the importation or exportation of a medical device is an offence under subsection 41MI(1), (4) or (5) or a contravention of section 41MIB; and
(b) the Secretary notifies the Comptroller‑General of Customs in writing that the Secretary wishes the Customs Act 1901 to apply to that importation or exportation;
the Customs Act 1901 has effect as if the device included in that importation or exportation were goods described as forfeited to the Crown under section 229 of that Act because they were:
(c) prohibited imports within the meaning of that Act; or
(d) prohibited exports within the meaning of that Act;
as the case requires.
41MK Wholesale supply of medical devices not included in the Register
A person commits an offence if:
(a) the person supplies a medical device in Australia; and
(b) none of the following subparagraphs applies in relation to the device:
(i) the device is of a kind included in the Register;
(ia) the device is of a kind covered by an exemption in force under section 41GS;
(ii) the device is an exempt device;
(iii) the device is the subject of an approval under section 41HB or an authority under section 41HC;
(iv) the device is the subject of an approval under subsection 41HD(1), (1A) or (2) that is held by the person; and
(c) the person to whom the device is supplied is not the ultimate consumer of the device.
Penalty: 120 penalty units.
41ML False advertising about medical devices
(1) A person commits an offence if:
(a) the person, by any means, advertises a medical device as being for a purpose; and
(b) the device is of a kind included in the Register; and
(c) the purpose is not a purpose accepted in relation to that inclusion; and
(d) either:
(i) the use of the medical device for the advertised purpose has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the medical device for the advertised purpose, if the medical device were so used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
(2) A person commits an offence if:
(a) the person, by any means, advertises a medical device as being for a purpose; and
(b) the device is of a kind included in the Register; and
(c) the purpose is not a purpose accepted in relation to that inclusion.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(3) A person commits an offence if:
(a) the person, by any means, advertises a medical device as being for a purpose; and
(b) the device is of a kind included in the Register; and
(c) the purpose is not a purpose accepted in relation to that inclusion.
Penalty: 100 penalty units.
(4) An offence against subsection (3) is an offence of strict liability.
41MLA Civil penalty for making misrepresentations about medical devices
(1) A person contravenes this section if:
(a) the person makes a representation of a kind referred to in subsection (2); and
(b) the representation is false or misleading.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
(2) Subsection (1) applies to the following representations:
(a) representations that medical devices are of a kind included in the Register;
(b) representations that medical devices are exempt devices;
(c) representations that medical devices are the subject of an approval under section 41HB or an authority under section 41HC;
(d) representations that medical devices are the subject of an approval under subsection 41HD(1), (1A) or (2).
41MLB Civil penalty for false advertising about medical devices
A person contravenes this section if:
(a) the person, by any means, advertises a medical device as being for a purpose; and
(b) the device is of a kind included in the Register; and
(c) the purpose is not a purpose accepted in relation to that inclusion.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
41MN Criminal offences relating to breaches of conditions
Offences relating to breaching a condition of the inclusion of a kind of medical device in the Register
(1) A person commits an offence if:
(a) a kind of medical device is included in the Register in relation to the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the inclusion of the kind of device in the Register; and
(d) the act or omission has resulted in, will result in, or is likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) a kind of medical device is included in the Register in relation to the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the inclusion of the kind of device in the Register.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(4A) A person commits an offence if:
(a) a kind of medical device is included in the Register in relation to the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the inclusion of the kind of device in the Register.
Penalty: 100 penalty units.
(4B) An offence against subsection (4A) is an offence of strict liability.
Offences relating to breaching a condition of a conformity assessment certificate
(5) A person commits an offence if:
(a) a conformity assessment certificate is issued in respect of the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the conformity assessment certificate; and
(d) the act or omission has resulted in, will result in, or is likely to result in, harm or injury to a person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (8) instead: see section 53A.
(8) A person commits an offence if:
(a) a conformity assessment certificate is issued in respect of the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the conformity assessment certificate.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(8A) A person commits an offence if:
(a) a conformity assessment certificate is issued in respect of the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the conformity assessment certificate.
Penalty: 100 penalty units.
(8B) An offence against subsection (8A) is an offence of strict liability.
Offence relating to breaching a condition of an exemption or approval, or a condition applicable under regulations
(9) A person commits an offence if:
(a) the person does an act or omits to do an act; and
(b) the act or omission breaches:
(i) a condition of an exemption applicable under regulations made for the purposes of section 41HA; or
(ii) a condition of an approval under section 41HB; or
(iii) a condition applicable under regulations made for the purposes of subsection 41HB(7); or
(iv) a condition of an approval under subsection 41HD(1), (1A) or (2).
Penalty: 60 penalty units.
Offences relating to breaching a condition of a conformity assessment body determination
(10) An Australian corporation commits an offence if:
(a) the corporation does an act or omits to do an act; and
(b) the act or omission breaches a condition referred to in subsection 41EWA(5); and
(c) the act or omission has resulted in, will result in, or is likely to result in, harm or injury to any person.
Penalty: 20,000 penalty units.
(11) An Australian corporation commits an offence if:
(a) the corporation does an act or omits to do an act; and
(b) the act or omission breaches a condition referred to in subsection 41EWA(5).
Penalty: 5,000 penalty units.
(12) An Australian corporation commits an offence if:
(a) the corporation does an act or omits to do an act; and
(b) the act or omission breaches a condition referred to in subsection 41EWA(5).
Penalty: 500 penalty units.
(13) An offence against subsection (12) is an offence of strict liability.
41MNA Civil penalties for breaching conditions
(1) A person contravenes this subsection if:
(a) a kind of medical device is included in the Register in relation to the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the inclusion of the kind of device in the Register.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
(2) A person contravenes this subsection if:
(a) a conformity assessment certificate is issued in respect of the person; and
(b) the person does an act or omits to do an act; and
(c) the act or omission breaches a condition of the conformity assessment certificate.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
(3) An Australian corporation contravenes this subsection if:
(a) the corporation does an act or omits to do an act; and
(b) the act or omission breaches a condition referred to in subsection 41EWA(5).
Maximum civil penalty: 50,000 penalty units.
Division 3A—Offences and civil penalties related to exemptions under Part 4‑6A
41MNB Criminal offences for breaching a condition of an exemption
(1) A person commits an offence if:
(a) the person does an act or omits to do an act in relation to a medical device; and
(b) the device is of a kind covered by an exemption in force under section 41GS; and
(c) the act or omission results in the breach of a condition of the exemption; and
(d) the act or omission is likely to cause a serious risk to public health.
Penalty: Imprisonment for 5 years or 2,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) Strict liability applies to paragraph (1)(b).
Note: For strict liability, see section 6.1 of the Criminal Code.
(3) A person commits an offence if:
(a) the person does an act or omits to do an act in relation to a medical device; and
(b) the device is of a kind covered by an exemption in force under section 41GS; and
(c) the act or omission results in the breach of a condition of the exemption.
Penalty: Imprisonment for 4 years or 240 penalty units, or both.
(4) Strict liability applies to paragraph (3)(b).
Note: For strict liability, see section 6.1 of the Criminal Code.
(5) A person commits an offence if:
(a) the person does an act or omits to do an act in relation to a medical device; and
(b) the device is of a kind covered by an exemption in force under section 41GS; and
(c) the act or omission results in the breach of a condition of the exemption.
Penalty: 60 penalty units.
(6) An offence against subsection (5) is an offence of strict liability.
Note: For strict liability, see section 6.1 of the Criminal Code.
41MNC Civil penalty for breaching a condition of an exemption
A person contravenes this section if:
(a) the person does an act or omits to do an act in relation to a medical device; and
(b) the device is of a kind covered by an exemption in force under section 41GS; and
(c) the act or omission results in the breach of a condition of the exemption.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
41MND Civil penalty for making misrepresentations about medical devices
A person contravenes this section if:
(a) the person makes a representation that medical devices are of a kind covered by an exemption in force under section 41GS; and
(b) the representation is false or misleading.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Division 4—Other offences and civil penalty provisions
41MO Criminal offences for misusing medical devices exempted for special or experimental uses
(1) A person commits an offence if:
(a) the person has been granted an authority under subsection 41HC(1) relating to a specified kind of medical device; and
(b) the person supplies a medical device of that kind:
(i) otherwise than in accordance with the authority; or
(ii) otherwise than in accordance with any conditions to which the authority is subject; or
(iii) otherwise than in accordance with any regulations made for the purpose of subsection 41HC(5); and
(c) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(d) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because:
(i) the supply is not in accordance with the authority; or
(ii) the supply is not in accordance with the conditions to which the authority is subject; or
(iii) the supply is not in accordance with regulations made for the purpose of subsection 41HC(5).
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (4) instead: see section 53A.
(4) A person commits an offence if:
(a) the person has been granted an authority under subsection 41HC(1) relating to a specified kind of medical device; and
(b) the person supplies a medical device of that kind:
(i) otherwise than in accordance with the authority; or
(ii) otherwise than in accordance with any conditions to which the authority is subject; or
(iii) otherwise than in accordance with any regulations made for the purpose of subsection 41HC(5).
Penalty: 500 penalty units.
(4AA) A person commits an offence if:
(a) the person has been granted an authority under subsection 41HC(1) relating to a specified kind of medical device; and
(b) the person supplies a medical device of that kind:
(i) otherwise than in accordance with the authority; or
(ii) otherwise than in accordance with any conditions to which the authority is subject; or
(iii) otherwise than in accordance with any regulations made for the purpose of subsection 41HC(5).
Penalty: 100 penalty units.
(4AB) An offence against subsection (4AA) is an offence of strict liability.
(4A) A person commits an offence if:
(a) the person is a health practitioner; and
(b) the person is included in a class of health practitioners specified in subsection 41HC(6) rules; and
(c) the person supplies a medical device of a kind specified in those rules; and
(d) any of the following applies:
(i) the supply is not in accordance with those rules;
(ii) the supply is not in the circumstances specified in those rules;
(iii) the supply is not in accordance with the conditions specified in those rules; and
(e) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person; and
(f) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because:
(i) the supply is not in accordance with those rules; or
(ii) the supply is not in the circumstances specified in those rules; or
(iii) the supply is not in accordance with the conditions specified in those rules.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
(4C) A person commits an offence if:
(a) the person is a health practitioner; and
(b) the person is included in a class of health practitioners specified in subsection 41HC(6) rules; and
(c) the person supplies a medical device of a kind specified in those rules; and
(d) any of the following applies:
(i) the supply is not in accordance with those rules;
(ii) the supply is not in the circumstances specified in those rules;
(iii) the supply is not in accordance with the conditions specified in those rules.
Penalty: 500 penalty units.
(4D) A person commits an offence if:
(a) the person is a health practitioner; and
(b) the person is included in a class of health practitioners specified in subsection 41HC(6) rules; and
(c) the person supplies a medical device of a kind specified in those rules; and
(d) any of the following applies:
(i) the supply is not in accordance with those rules;
(ii) the supply is not in the circumstances specified in those rules;
(iii) the supply is not in accordance with the conditions specified in those rules.
Penalty: 100 penalty units.
(4E) An offence against subsection (4D) is an offence of strict liability.
(5) A person commits an offence if:
(a) the person has been granted an approval under section 41HB relating to a specified medical device or specified kind of medical device; and
(b) the person uses a medical device of that kind:
(i) in the treatment of another person; or
(ii) solely for experimental purposes in humans;
otherwise than in accordance with the approval; and
(c) either:
(i) the use of the device has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the device, if the device were used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (8) instead: see section 53A.
(8) A person commits an offence if:
(a) the person has been granted an approval under section 41HB relating to a specified medical device or specified kind of medical device; and
(b) the person uses a medical device of that kind:
(i) in the treatment of another person; or
(ii) solely for experimental purposes in humans;
otherwise than in accordance with the approval.
Penalty: 500 penalty units.
(9) A person commits an offence if:
(a) the person has been granted an approval under section 41HB relating to a specified medical device or specified kind of medical device; and
(b) the person uses a medical device of that kind:
(i) in the treatment of another person; or
(ii) solely for experimental purposes in humans;
otherwise than in accordance with the approval.
Penalty: 100 penalty units.
(10) An offence against subsection (9) is an offence of strict liability.
41MP Criminal offence for failing to notify adverse events etc.
(1) A person commits an offence if:
(a) the person is a person in relation to whom a kind of medical device is included in the Register; and
(b) the person knows that particular information is information of a kind mentioned in subsection (2); and
(c) the person fails to give that information to the Secretary within the period specified in the regulations (whether or not the person has already given to the Secretary other information relating to the same matter).
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) The information with which subsection (1) is concerned is information of the following kinds:
(a) information relating to:
(i) any malfunction or deterioration in the characteristics or performance of the kind of device; or
(ii) any inadequacy in the design, production, labelling, instructions for use or advertising materials of the kind of device; or
(iii) any use in accordance with, or contrary to, the use intended by the manufacturer of the kind of device;
that might lead, or might have led, to the death of a patient or a user of the device, or to a serious deterioration in his or her state of health;
(b) information relating to any technical or medical reason for a malfunction or deterioration of a kind referred to in subparagraph (a)(i) that has led the manufacturer to take steps to recall devices of that kind that have been distributed;
(c) information that indicates that a device of that kind does not comply with the essential principles;
(d) information that indicates that a certificate or other document (other than a certificate or other document issued by the Secretary under this Act) used for the purpose of an application under subsection 41FC(1) to signify:
(i) compliance with the essential principles; or
(ii) the application of relevant conformity assessment procedures to a device of that kind or the application of requirements, comparable to those procedures, to a device of that kind;
has been restricted, suspended, revoked or is no longer in effect.
41MPA Civil penalty for failing to notify adverse events etc.
(1) A person contravenes this section if:
(a) a kind of medical device is included in the Register in relation to the person; and
(b) the information is of a kind mentioned in subsection (2); and
(c) the person does not give information of a kind mentioned in subsection (2) to the Secretary within the period specified in the regulations (whether or not the person has already given to the Secretary other information relating to the same matter).
Maximum civil penalty:
(a) for an individual—3,000 penalty units; and
(b) for a body corporate—30,000 penalty units.
(2) The information with which subsection (1) is concerned is information of the following kinds:
(a) information relating to:
(i) any malfunction or deterioration in the characteristics or performance of the kind of device; or
(ii) any inadequacy in the design, production, labelling, instructions for use or advertising materials of the kind of device; or
(iii) any use in accordance with, or contrary to, the use intended by the manufacturer of the kind of device;
that might lead, or might have led, to the death of a patient or user of the device, or to a serious deterioration in his or her state of health;
(b) information relating to any technical or medical reason for a malfunction or deterioration of a kind referred to in subparagraph (a)(i) that has led the manufacturer to take steps to recall devices of that kind that have been distributed;
(c) information that indicates that a device of that kind does not comply with the essential principles;
(d) information that indicates that a certificate or other document (other than a certificate or other document issued by the Secretary under this Act) used for the purpose of an application under subsection 41FC(1) to signify:
(i) compliance with the essential principles; or
(ii) the application of relevant conformity assessment procedures to a device of that kind or the application of requirements, comparable to those procedures, to a device of that kind;
has been restricted, suspended, revoked or is no longer in effect.
41MPB Relief from liability for contraventions for failing to notify adverse events etc.
(1) If:
(a) proceedings for the contravention of section 41MPA (a civil penalty provision) are brought against a person; and
(b) in the proceedings it appears to the Court that the person has, or may have, contravened that section but that:
(i) the person has a reasonable excuse; and
(ii) having regard to all the circumstances of the case, the person ought fairly to be excused for the contravention;
the Court may relieve the person either wholly or partly from a liability to which the person would otherwise be subject, or that might otherwise be imposed on the person, because of the contravention.
(2) If a person thinks that proceedings for the contravention of section 41MPA will or may be begun against them, they may apply to the Court for relief.
(3) On an application under subsection (2), the Court may grant relief under subsection (1) as if proceedings had been begun in the Court.
(4) For the purposes of subsection (2) as applying for the purposes of a case tried by a judge with a jury:
(a) a reference in that subsection to the Court is a reference to the judge; and
(b) the relief that may be granted includes withdrawing the case in whole or in part from the jury and directing judgment to be entered for the person on such terms as to costs as the judge thinks appropriate.
41MQ Notification of adverse events etc. where application withdrawn or lapses
(1) If an application for inclusion of a kind of medical device in the Register is withdrawn or lapses, the Secretary may give the applicant written notice requiring the applicant:
(a) to inform the Secretary in writing whether the applicant is aware of any information of a kind mentioned in subsection 41MP(2) or 41MPA(2) relating to the kind of device; and
(b) if the applicant is aware of such information, to give the information to the Secretary in writing.
(2) Notice under subsection (1) may only be given within 10 working days after an application is withdrawn or lapses.
(3) A person commits an offence if the person fails to comply with the requirements of a notice under subsection (1) within 20 working days after the notice is given to the person.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(4) A person commits an offence if:
(a) the person gives information in purported compliance with a notice under this section; and
(b) the information is false or misleading in a material particular.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
41MR Civil penalties for failing to notify adverse effects etc. where application withdrawn or lapses
Civil penalty for failing to comply with requirements of a notice
(1) A person contravenes this subsection if the person does not comply with the requirements of a notice under subsection 41MQ(1) within 20 working days after the day on which the notice is given to the person.
Maximum civil penalty:
(a) for an individual—3,000 penalty units; and
(b) for a body corporate—30,000 penalty units.
Civil penalty for giving false or misleading information in purported compliance with requirements of a notice
(2) A person contravenes this subsection if:
(a) the person gives information in purported compliance with a notice under subsection 41MQ(1); and
(b) the information is false or misleading in a material particular.
Maximum civil penalty:
(a) for an individual—3,000 penalty units; and
(b) for a body corporate—30,000 penalty units.
Chapter 5—Advertising, counterfeit therapeutic goods and product tampering
Part 5‑1—Advertising and generic information
Division 1—Preliminary
42AA This Part not to apply to advertisements directed at health professionals etc.
(1) This Part does not apply to advertisements directed exclusively to:
(a) medical practitioners, psychologists, dentists, pharmacists, optometrists, chiropractors, physiotherapists, nurses, midwives, dental hygienists, dental prosthetists, dental therapists or osteopaths; or
(b) persons who are:
(i) engaged in the business of wholesaling therapeutic goods; or
(ii) purchasing officers in hospitals; or
(c) herbalists, homoeopathic practitioners, naturopaths, nutritionists, practitioners of traditional Chinese medicine or podiatrists registered under a law of a State or Territory; or
(d) a class of persons specified under subsection (1A).
(1A) The Minister may, by legislative instrument, specify a class of persons for the purposes of paragraph (1)(d).
(2) This Part does not apply to advertisements directed exclusively to persons who are members of an Australian branch (however described) of one of the bodies prescribed for the purposes of this subsection.
(3) For the purposes of subsection (2), a person is taken to be a member of an Australian branch of one of those bodies if, and only if, the person has the qualifications and training that are necessary or appropriate for membership of the relevant body.
(4) This Part does not apply to advice or information given directly to a patient by a person referred to in paragraph (1)(a) or (c) or subsection (2) in the course of treatment of that patient.
42AB This Part not to apply to advertisements for goods not for human use
This Part does not apply to advertisements in respect of goods that are not for use in humans.
42AC This Part not to apply to advertisements for exported goods
(1) Subject to subsection (2), this Part does not apply to advertisements solely for therapeutic goods that have been exported or are intended exclusively for export.
(2) Sections 42DKB, 42DLA and 42DLC and Divisions 5 and 6 apply in relation to advertisements of that kind.
42B Definitions
In this Part, unless the contrary intention appears:
generic information, in relation to therapeutic goods, includes any statement, pictorial representation or design, however made, about the composition, properties or other characteristics of therapeutic goods, but does not include:
(a) an advertisement about the goods; or
(b) generic information included in an advertisement about the goods; or
(c) bona fide news.
prohibited representation means a representation referred to in subsection 42DJ(1).
required representation means a representation referred to in subsection 42DJ(2).
restricted representation means a representation referred to in section 42DD.
42BAA Therapeutic Goods Advertising Code
(1) The Minister may, by legislative instrument, make a code relating to advertisements about therapeutic goods.
(2) Despite subsection 14(2) of the Legislation Act 2003, an instrument under subsection (1) of this section may make provision in relation to a matter by applying, adopting or incorporating, with or without modification, any matter contained in an instrument or other writing as in force or existing from time to time.
Division 3—General provisions about advertising therapeutic goods
42DA Simplified outline of this Division
Representations in advertisements about therapeutic goods may be restricted representations, required representations or prohibited representations. The offences and civil penalties in Division 3A refer to these 3 kinds of representations.
42DB Definitions
In this Division:
applicant means an applicant for approval of the use of a restricted representation in an advertisement about therapeutic goods.
approval holder, in relation to a restricted representation, means the person to whom notice of approval of the use of the restricted representation was given.
42DD Restricted representations
For the purposes of this Part, a representation in an advertisement about therapeutic goods that refers to a form of a disease, condition, ailment or defect identified in a part of the Therapeutic Goods Advertising Code as a serious form of a disease, condition, ailment or defect is a restricted representation.
Note: See sections 42DL and 42DLB for offences and a civil penalty for advertising therapeutic goods, where the advertisement contains a restricted representation.
42DE Applications for approval of use of restricted representation
(1) An application for approval of the use of a restricted representation must be made to the Secretary in accordance with a form approved, in writing, by the Secretary.
(2) An approval of a form may require or permit an application to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
42DF Approval of use of restricted representation
(1) If an application for approval of the use of a restricted representation is made, the Secretary must approve the use of the restricted representation if the Secretary is satisfied that:
(a) the representation is accurate and balanced; and
(b) the representation is not misleading or likely to be misleading.
(2) Otherwise, the Secretary must refuse to approve the use of the restricted representation.
(3) An approval may be subject to conditions imposed by the Secretary.
(4) In deciding whether to approve or refuse to approve the use of a restricted representation, the Secretary must take into consideration:
(b) any advice of a committee that is established under the regulations and is prescribed by the regulations for the purposes of this paragraph; and
(c) the public interest criteria mentioned in the part of the Therapeutic Goods Advertising Code dealing with restricted representations.
42DG Notice of approval or refusal
(1) The Secretary must give written notice to the applicant of the approval of, or of the refusal to approve, the use of a restricted representation.
(2) If written notice is not given to the applicant within the period of 60 days after the day on which the application was made (or within such longer period as the Secretary specifies by written notice to the applicant before the end of that period), the Secretary is taken to have approved the use of the restricted representation at the end of the period.
(3) If an approval is subject to conditions, the conditions must be set out in the notice.
(4) A notice of refusal to approve the use of a restricted representation must:
(a) give the Secretary’s reasons for the refusal; and
(b) inform the applicant of the applicant’s right to have the Secretary’s decision reviewed by the Minister under section 60.
42DH Variation of conditions of approval
(1) The Secretary, by written notice to an approval holder, may vary any condition of approval of the use of a restricted representation.
(2) The notice must:
(a) give the Secretary’s reasons for the variation; and
(b) inform the approval holder of the approval holder’s right to have the Secretary’s decision reviewed by the Minister under section 60.
42DI Withdrawal of approval
(1) The Secretary, by written notice, may withdraw the approval of the use of a restricted representation if:
(a) the Secretary is satisfied that:
(i) information given by the applicant in the application was false or incorrect and the Secretary, or the Minister on review of a decision of the Secretary under section 42DF or 42DH, relied on the information in deciding to approve the use of the representation; or
(ii) the restricted representation has become a prohibited representation; or
(iii) there has been a breach of a condition of approval; or
(b) both:
(i) additional information about the safety of the therapeutic goods becomes available; and
(ii) the Secretary is satisfied that, if that information had been available at the time of the approval, the Secretary would not have approved the use of the restricted representation; or
(c) the use of the restricted representation is permitted under subsection 42DK(1).
(2) The notice must:
(a) give the Secretary’s reasons for the withdrawal; and
(b) inform the approval holder of the approval holder’s right to have the Secretary’s decision reviewed by the Minister under section 60.
42DJ Prohibited and required representations
(1) For the purposes of this Part, representations of a kind specified in regulations made for the purposes of this subsection are prohibited representations about therapeutic goods of a kind specified in those regulations.
(2) For the purposes of this Part, representations of a kind specified in regulations made for the purposes of this subsection are required representations about the therapeutic goods of a kind specified in those regulations.
42DK Permitted use of restricted or prohibited representations
Restricted representations
(1) The Secretary may, by writing, permit the use of specified restricted representations in specified advertisements about specified therapeutic goods.
Prohibited representations
(2) The Secretary may, by writing, permit the use of specified prohibited representations:
(a) on the label of specified therapeutic goods; or
(b) on the package in which specified therapeutic goods are contained; or
(c) on any material included with the package in which specified therapeutic goods are contained;
if the Secretary is satisfied that the representations are necessary for the appropriate use of the goods.
(3) The Secretary may, by writing, permit the use of specified prohibited representations in specified advertisements about specified therapeutic goods if the Secretary is satisfied that the representations are necessary in the interests of public health.
Conditions
(4) A permission under this section may be subject to conditions specified in the permission.
Permission not a legislative instrument
(5) A permission under this section is not a legislative instrument.
Publication
(6) As soon as practicable after giving a permission under this section, the Secretary must cause the permission to be published on the Department’s website.
Division 3A—Advertising offences and civil penalties
42DKB Certain representations not to be advertised
(1) If a representation in an advertisement about therapeutic goods is false or misleading, the Secretary may, by notice given to a person apparently responsible for:
(a) advertising the therapeutic goods; or
(b) causing the advertising of the therapeutic goods;
prevent that person from advertising the therapeutic goods, or causing the advertising of the therapeutic goods, in circumstances where the advertisement contains that representation (whether in express terms or by necessary implication).
Note: See sections 42DLA and 42DLC for criminal offences and a civil penalty for contravening the notice.
(2) A notice under subsection (1) is not a legislative instrument.
Publication
(3) As soon as practicable after giving a notice under subsection (1), the Secretary must cause the notice to be published on the Department’s website.
42DL Advertising offences—general
(1) A person commits an offence if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) subsection (5), (6), (7), (8), (9), (10), (11) or (12) applies to the advertisement; and
(c) either:
(i) the use of the goods in reliance on the advertisement has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the goods in reliance on the advertisement, if the goods were so used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
(2) A person commits an offence if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) subsection (5), (6), (7), (8), (9), (10), (11) or (12) applies to the advertisement.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(3) A person commits an offence if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) subsection (5), (6), (7), (8), (9), (10), (11) or (12) applies to the advertisement.
Penalty: 100 penalty units.
(4) An offence against subsection (3) is an offence of strict liability.
Contravening provisions
(5) This subsection applies to the advertisement if it contains a prohibited representation (whether in express terms or by necessary implication) about the goods and either of the following applies:
(a) no permission under section 42DK is in force in relation to the prohibited representation;
(b) a permission under section 42DK is in force in relation to the prohibited representation but the use of the prohibited representation is not in accordance with the permission or a condition of the permission.
(6) This subsection applies to the advertisement if it does not contain a required representation about the goods.
(7) This subsection applies to the advertisement if it contains a restricted representation (whether in express terms or by necessary implication) and either of the following applies:
(a) neither an approval under section 42DF nor a permission under section 42DK is in force in relation to the restricted representation;
(b) an approval under section 42DF or a permission under section 42DK is in force in relation to the restricted representation but the use of the restricted representation is not in accordance with the approval or permission or a condition of the approval or permission.
(8) This subsection applies to the advertisement if it contains a reference to this Act, other than in a statement of the registration number, listing number or device number of the goods.
(9) This subsection applies to the advertisement if it contains a statement, pictorial representation or design suggesting or implying the goods have been recommended or approved by or on behalf of a government or government authority (including a foreign government or foreign government authority), other than:
(a) a statement of the availability of the goods as a pharmaceutical benefit; or
(b) a statement, pictorial representation or design authorised or required by a government or government authority (not including a foreign government or foreign government authority); or
(c) a statement, pictorial representation or design prescribed by the regulations for the purposes of this paragraph.
(10) This subsection applies to the advertisement if it refers to substances, or goods containing substances, included in Schedule 3, 4 or 8 to the current Poisons Standard but not in Appendix H of the current Poisons Standard, other than a reference authorised or required by a government or government authority (not including a foreign government or foreign government authority).
(11) This subsection applies to the advertisement if it refers to a biological, other than a reference authorised or required by a government or government authority (not including a foreign government or foreign government authority).
(12) This subsection applies to the advertisement if it refers to therapeutic goods that are not entered in the Register and that are prescribed by the regulations for the purposes of this subsection, other than a reference authorised or required by a government or government authority (not including a foreign government or foreign government authority).
Continuing offences
(13) A person who contravenes subsection (1), (2) or (3) commits a separate offence in respect of each day (including a day of a conviction for the offence or any later day) during which the contravention continues.
(14) The maximum penalty for each day that an offence against subsection (1), (2) or (3) continues is 10% of the maximum pecuniary penalty that can be imposed in respect of that offence.
42DLA Advertising offences—contravening section 42DKB notice
(1) A person commits an offence if:
(a) the Secretary has given a notice to the person under section 42DKB in relation to therapeutic goods; and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the notice; and
(d) either:
(i) the use of the goods has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the goods, if the goods were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because of the contravention.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
(2) A person commits an offence if:
(a) the Secretary has given a notice to the person under section 42DKB; and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the notice.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(3) A person commits an offence if:
(a) the Secretary has given a notice to the person under section 42DKB; and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the notice.
Penalty: 100 penalty units.
(4) An offence against subsection (3) is an offence of strict liability.
42DLB Civil penalty relating to advertisements—general
(1) A person contravenes this subsection if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) subsection (2), (3), (4), (5), (6), (7), (8) or (9) applies to the advertisement.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Contravening provisions
(2) This subsection applies to the advertisement if it contains a prohibited representation (whether in express terms or by necessary implication) about the goods and either of the following applies:
(a) no permission under section 42DK is in force in relation to the prohibited representation;
(b) a permission under section 42DK is in force in relation to the prohibited representation but the use of the prohibited representation is not in accordance with the permission or a condition of the permission.
(3) This subsection applies to the advertisement if it does not contain a required representation about the goods.
(4) This subsection applies to the advertisement if it contains a restricted representation (whether in express terms or by necessary implication) and either of the following applies:
(a) neither an approval under section 42DF nor a permission under section 42DK is in force in relation to the restricted representation;
(b) an approval under section 42DF or a permission under section 42DK is in force in relation to the restricted representation but the use of the restricted representation is not in accordance with the approval or permission or a condition of the approval or permission.
(5) This subsection applies to the advertisement if it contains a reference to this Act, other than in a statement of the registration number, listing number or device number of the goods.
(6) This subsection applies to the advertisement if it contains a statement, pictorial representation or design suggesting or implying the goods have been recommended or approved by or on behalf of a government or government authority (including a foreign government or foreign government authority), other than:
(a) a statement of the availability of the goods as a pharmaceutical benefit; or
(b) a statement, pictorial representation or design authorised or required by a government or government authority (not including a foreign government or foreign government authority); or
(c) a statement, pictorial representation or design prescribed by the regulations for the purposes of this paragraph.
(7) This subsection applies to the advertisement if it refers to substances, or goods containing substances, included in Schedule 3, 4 or 8 to the current Poisons Standard but not in Appendix H of the current Poisons Standard, other than a reference authorised or required by a government or government authority (not including a foreign government or foreign government authority).
(8) This subsection applies to the advertisement if it refers to a biological, other than a reference authorised or required by a government or government authority (not including a foreign government or foreign government authority).
(9) This subsection applies to the advertisement if it refers to therapeutic goods that are not entered in the Register and that are prescribed by the regulations for the purposes of this subsection, other than a reference authorised or required by a government or government authority (not including a foreign government or foreign government authority).
Exception
(10) Subsection (1) does not apply if:
(a) the person is a broadcaster, a datacaster, the SBS or a person of a kind prescribed by the regulations for the purposes of this paragraph; and
(b) as a result of steps taken by the person, it was reasonable for the person to assume that subsections (2) to (9) did not apply to the advertisement.
(11) In this section:
broadcaster has the meaning given by clause 3 of Schedule 2 to the Broadcasting Services Act 1992.
datacaster means a person who holds a datacasting licence (within the meaning of the Broadcasting Services Act 1992).
SBS has the same meaning as in the Special Broadcasting Service Act 1991.
42DLC Civil penalty relating to advertisements—contravening section 42DKB notice
A person contravenes this section if:
(a) the Secretary has given a notice to the person under section 42DKB; and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the notice.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
42DM Offences—non‑compliance with the Therapeutic Goods Advertising Code
(1) A person commits an offence if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) the advertisement does not comply with the Therapeutic Goods Advertising Code; and
(c) either:
(i) the use of the goods in reliance on the advertisement has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the goods in reliance on the advertisement, if the goods were so used, would result in, or would be likely to result in, harm or injury to any person.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
(2) A person commits an offence if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) the advertisement does not comply with the Therapeutic Goods Advertising Code.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(3) A person commits an offence if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) the advertisement does not comply with the Therapeutic Goods Advertising Code.
Penalty: 100 penalty units.
(4) An offence against subsection (3) is an offence of strict liability.
Continuing offences
(5) A person who contravenes subsection (1), (2) or (3) commits a separate offence in respect of each day (including a day of a conviction for the offence or any later day) during which the contravention continues.
(6) The maximum penalty for each day that an offence against subsection (1), (2) or (3) continues is 10% of the maximum pecuniary penalty that can be imposed in respect of that offence.
42DMA Civil penalty—non‑compliance with the Therapeutic Goods Advertising Code
(1) A person contravenes this section if:
(a) the person:
(i) advertises, by any means, therapeutic goods; or
(ii) causes the advertising, by any means, of therapeutic goods; and
(b) the advertisement does not comply with the Therapeutic Goods Advertising Code.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Exception
(2) Subsection (1) does not apply if:
(a) the person is a broadcaster, a datacaster, the SBS or a person of a kind prescribed by the regulations for the purposes of this paragraph; and
(b) as a result of steps taken by the person, it was reasonable for the person to assume that the advertisement complied with the Therapeutic Goods Advertising Code.
(3) In this section:
broadcaster has the meaning given by clause 3 of Schedule 2 to the Broadcasting Services Act 1992.
datacaster means a person who holds a datacasting licence (within the meaning of the Broadcasting Services Act 1992).
SBS has the same meaning as in the Special Broadcasting Service Act 1991.
Division 4—Generic information about ingredients or components of therapeutic goods
42DN Application of Division
This Division applies to generic information about goods that:
(a) may be used as an ingredient or component in the manufacture of therapeutic goods; and
(b) although not presented for supply as therapeutic goods, come within the meaning of therapeutic goods because they are represented to be:
(i) for therapeutic use; or
(ii) for use as an ingredient or component in the manufacture of other therapeutic goods.
42DO Compliance with the Code
Generic information to which this Division applies must comply with the provisions of the Therapeutic Goods Advertising Code that are prescribed by the regulations for the purposes of this section as if those provisions applied to generic information in the same way as they apply to advertisements.
42DP Offences—dissemination of generic information
(1) A person commits an offence if:
(a) the person disseminates, by any means, generic information about therapeutic goods to the public or a section of the public; and
(b) the dissemination of that generic information does not comply with the provisions of the Therapeutic Goods Advertising Code that are prescribed by regulations for the purposes of section 42DO.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(2) A person commits an offence if:
(a) the person disseminates, by any means, generic information about therapeutic goods to the public or a section of the public; and
(b) the dissemination of that generic information does not comply with the provisions of the Therapeutic Goods Advertising Code that are prescribed by regulations for the purposes of section 42DO.
Penalty: 100 penalty units.
(3) An offence against subsection (2) is an offence of strict liability.
42DQ Civil penalty for dissemination of generic information
A person contravenes this section if:
(a) the person disseminates, by any means, generic information about therapeutic goods to the public or a section of the public; and
(b) the dissemination of that generic information does not comply with the provisions of the Therapeutic Goods Advertising Code that are prescribed by regulations for the purposes of section 42DO.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Division 5—Secretary may require information or documents
42DR Secretary may require information or documents
Advertisements
(1) The Secretary may, by written notice given to a person apparently responsible for advertising therapeutic goods, or for causing the advertising of therapeutic goods, require the person to give to the Secretary specified information, or to produce to the Secretary specified documents, relating to the advertisement.
Generic information
(2) The Secretary may, by written notice given to a person apparently responsible for disseminating, or for causing the disseminating of, generic information about therapeutic goods to the public or a section of the public, require the person to give to the Secretary specified information, or to produce to the Secretary specified documents, relating to the dissemination.
Manner of compliance
(3) The person must give the information, or produce the documents, to the Secretary:
(a) within the period, of not less than 14 days after the day the notice is given, specified in the notice or within such longer period as the Secretary allows; and
(b) in the form specified in the notice.
Note: Section 42DS contains criminal offences for failing to comply with the notice and for giving false or misleading information or documents and section 42DT contains a civil penalty for giving false or misleading information or documents.
(4) The form may require or permit the information to be given, or the documents to be produced, in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
Notice not a legislative instrument
(5) A notice under subsection (1) or (2) is not a legislative instrument.
42DS Criminal offences for failing to comply with a notice etc.
(1) A person commits an offence if:
(a) the person is given a notice under section 42DR; and
(b) the person fails to comply with the notice.
Penalty: 500 penalty units.
(2) A person commits an offence if:
(a) the person is given a notice under section 42DR; and
(b) the person fails to comply with the notice.
Penalty: 100 penalty units.
(3) An offence against subsection (2) is an offence of strict liability.
(4) A person commits an offence if:
(a) the person is given a notice under section 42DR; and
(b) the person gives information or produces a document in compliance or purported compliance with the notice; and
(c) the information or document is false or misleading in a material particular.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(5) A person commits an offence if:
(a) the person is given a notice under section 42DR; and
(b) the person gives information or produces a document in compliance or purported compliance with the notice; and
(c) the information or document is false or misleading in a material particular.
Penalty: 100 penalty units.
(6) An offence against subsection (5) is an offence of strict liability.
42DT Civil penalty for giving false or misleading information or document in compliance with a notice
A person contravenes this section if:
(a) the person is given a notice under section 42DR; and
(b) the person gives information or produces a document in compliance or purported compliance with the notice; and
(c) the information or document is false or misleading in a material particular.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
42DU Self‑incrimination
(1) A person is not excused from giving information or producing a document under section 42DR on the ground that the information or the production of the document might tend to incriminate the person or expose the person to a penalty.
(2) However, in the case of an individual:
(a) the information given or the document produced; and
(b) giving the information or producing the document; and
(c) any information, document or thing obtained as a direct or indirect consequence of giving the information or producing the document;
are not admissible in evidence against the individual:
(d) in criminal proceedings, except proceedings for an offence against subsection 42DS(4) or (5); or
(e) in civil proceedings, except proceedings under section 42Y for a contravention of section 42DT.
Division 6—Directions about advertisements or generic information
42DV Directions about advertisements or generic information
Advertisements
(1) If, in relation to the advertising of therapeutic goods, the Secretary is satisfied that there has been a contravention of this Act or the regulations, the Secretary may, in writing, direct a person apparently responsible for advertising the therapeutic goods, or for causing the advertising of the therapeutic goods, to do one or more of the following:
(a) cease the advertisement;
(b) make a retraction;
(c) make a correction;
(d) recover any advertisement that is still in circulation;
(e) destroy the advertisement;
(f) cease making a particular claim or representation made by the advertisement.
Generic information
(2) If, in relation to the dissemination of generic information about therapeutic goods to the public or a section of the public, the Secretary is satisfied that there has been a contravention of this Act or the regulations, the Secretary may, in writing, direct a person apparently responsible for the dissemination, or for causing the dissemination, to do one or more of the following:
(a) withdraw the generic information;
(b) make a retraction;
(c) make a correction;
(d) recover any generic information that is still in circulation;
(e) destroy the generic information;
(f) cease making a particular claim or representation made by the generic information.
Conditions
(3) A direction under subsection (1) or (2) may be subject to conditions specified in the direction.
(4) Without limiting subsection (3), the conditions may relate to one or more of the following:
(a) the period for doing a thing the subject of the direction;
(b) in relation to the making of a retraction or correction, either or both of the following:
(i) the form and manner of the retraction or correction;
(ii) the period for which the retraction or correction must be made publicly available;
(c) the reporting to the Secretary of compliance with the direction.
Direction not a legislative instrument
(5) A direction under subsection (1) or (2) is not a legislative instrument.
Publication
(6) As soon as practicable after giving a direction under subsection (1) or (2), the Secretary must cause the direction to be published on the Department’s website.
42DW Offences—contravening direction under section 42DV
(1) A person commits an offence if:
(a) the Secretary has given a direction to the person under subsection 42DV(1) or (2) in relation to therapeutic goods; and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the direction or a condition of the direction; and
(d) either:
(i) the use of the goods has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the goods, if the goods were used, would result in, or would be likely to result in, harm or injury to any person; and
(e) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because of the contravention.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
(2) A person commits an offence if:
(a) the Secretary has given a direction to the person under subsection 42DV(1) or (2); and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the direction or a condition of the direction.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(3) A person commits an offence if:
(a) the Secretary has given a direction to the person under subsection 42DV(1) or (2); and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the direction or a condition of the direction.
Penalty: 100 penalty units.
(4) An offence against subsection (3) is an offence of strict liability.
42DX Civil penalty for contravening direction under section 42DV
A person contravenes this section if:
(a) the Secretary has given a direction to the person under subsection 42DV(1) or (2); and
(b) the person does an act or omits to do an act; and
(c) the act or omission contravenes the direction or a condition of the direction.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
Division 7—Public warning notices
42DY Secretary may issue a public warning notice
(1) The Secretary may issue to the public a written notice containing a warning about therapeutic goods if:
(a) the Secretary reasonably suspects that there has been a contravention of this Act or the regulations in relation to:
(i) the advertising of the therapeutic goods; or
(ii) the dissemination of generic information about the therapeutic goods to the public or a section of the public; and
(b) the Secretary is satisfied that it is in the public interest to issue the notice.
(2) If:
(a) the Secretary gives a person a notice (the substantiation notice) under subsection 42DR(1) or (2); and
(b) the person fails to comply with the substantiation notice; and
(c) the Secretary is satisfied that it is in the public interest to issue a notice under this subsection;
the Secretary may issue to the public a written notice containing a warning that the person has failed to comply with the substantiation notice, and specifying the matter to which the substantiation notice related.
(3) Subsection (2) does not limit subsection (1).
(4) A notice under this section is not a legislative instrument.
Part 5‑2—Counterfeit therapeutic goods
42E Offence of dealing with counterfeit therapeutic goods
(1) A person commits an offence if:
(a) the person intentionally:
(i) manufactures goods in Australia; or
(ii) supplies goods in Australia; or
(iii) imports goods into Australia; or
(iv) exports goods from Australia; and
(b) the goods are therapeutic goods; and
(c) the goods are counterfeit and the person knows that fact or is reckless as to whether that fact exists.
Penalty: 7 years imprisonment or 2,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) Goods are counterfeit if any of the following contain a false representation of a matter listed in subsection (3):
(a) the label or presentation of the goods;
(b) any document or record relating to the goods or their manufacture;
(c) any advertisement for the goods.
(3) The matters are as follows:
(a) the identity or name of the goods;
(b) the formulation, composition or design specification of the goods or of any ingredient or component of them;
(c) the presence or absence of any ingredient or component of the goods;
(d) the strength or size of the goods (other than the size of any pack in which the goods are contained);
(e) the strength or size of any ingredient or component of the goods;
(f) the sponsor, source, manufacturer or place of manufacture of the goods.
(5) To avoid doubt, a term that is defined in subsection 3(1) in relation to therapeutic goods and used in this section in relation to goods has in this section the meaning given by subsection 3(1).
42EA Civil penalty relating to dealing with counterfeit therapeutic goods
A person contravenes this section if:
(a) the person does any of the following:
(i) manufactures goods in Australia;
(ii) supplies goods in Australia;
(iii) imports goods into Australia;
(iv) exports goods from Australia; and
(b) the goods are therapeutic goods; and
(c) the goods are counterfeit.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
42EB Relief from liability for certain contraventions relating to dealing with counterfeit therapeutic goods
(1) If:
(a) proceedings for the contravention of section 42EA (a civil penalty provision) are brought against a person; and
(b) in the proceedings it appears to the Court that the person has, or may have, contravened that section but that:
(i) the person has a reasonable excuse; and
(ii) having regard to all the circumstances of the case, the person ought fairly to be excused for the contravention;
the Court may relieve the person either wholly or partly from a liability to which the person would otherwise be subject, or that might otherwise be imposed on the person, because of the contravention.
(2) If a person thinks that proceedings for the contravention of section 42EA will or may be begun against them, they may apply to the Court for relief.
(3) On an application under subsection (2), the Court may grant relief under subsection (1) as if proceedings had been begun in the Court.
(4) For the purposes of subsection (2) as applying for the purposes of a case tried by a judge with a jury:
(a) a reference in that subsection to the Court is a reference to the judge; and
(b) the relief that may be granted includes withdrawing the case in whole or in part from the jury and directing judgment to be entered for the person on such terms as to costs as the judge thinks appropriate.
Exception
(5) This section does not apply to civil proceedings against a person for manufacturing therapeutic goods in Australia that are counterfeit (see subparagraph 42EA(a)(i)).
42F Customs treatment of counterfeit therapeutic goods
Imported counterfeit therapeutic goods
(1) If the Secretary notifies the Comptroller‑General of Customs in writing that the Secretary wishes the Customs Act 1901 to apply to an import of counterfeit therapeutic goods, that Act has effect as if the goods included in the import were goods described as forfeited to the Crown under section 229 of that Act because they were prohibited imports within the meaning of that Act.
Exported counterfeit therapeutic goods
(2) If the Secretary notifies the Comptroller‑General of Customs in writing that the Secretary wishes the Customs Act 1901 to apply to an export of counterfeit therapeutic goods, that Act has effect as if the goods included in the export were goods described as forfeited to the Crown under section 229 of that Act because they were prohibited exports within the meaning of that Act.
Part 5‑3—Product tampering
42T Notifying of actual or potential tampering
(1) A person commits an offence if:
(a) the person supplies, manufactures or is a sponsor of, or proposes to supply, manufacture or become a sponsor of, therapeutic goods; and
(b) either:
(i) the person knows that some or all of those therapeutic goods, or any other therapeutic goods, are or have been subject to actual or potential tampering; or
(ii) some or all of those therapeutic goods, or any other therapeutic goods, are or have been subject to actual or potential tampering, and the person is reckless as to that fact; and
(c) the person fails, within 24 hours after becoming aware of, or becoming aware of a substantial risk of, the actual or potential tampering, to notify the Secretary.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) A person commits an offence if:
(a) the person supplies, manufactures or is a sponsor of, or proposes to supply, manufacture or become a sponsor of, therapeutic goods; and
(b) the person receives information or a demand; and
(c) either:
(i) the person knows that the information or demand relates (either expressly or by implication) to actual or potential tampering with some or all of those therapeutic goods, or any other therapeutic goods; or
(ii) the information or demand relates (either expressly or by implication) to actual or potential tampering with some or all of those therapeutic goods, or any other therapeutic goods, and the person is negligent as to that fact; and
(d) the person fails to notify the Secretary of the information or demand within 24 hours after receiving it.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(3) For the purposes of subparagraph (2)(c)(ii), the person is only taken to be negligent as to the fact that the information or demand is of the kind referred to in that subparagraph if:
(a) the person’s acts or omissions involve such a great falling short of the standard of care that a reasonable person would exercise in the circumstances; and
(b) there is such a high risk that the information or demand is of that kind;
that the acts or omissions merit criminal punishment.
(4) For the purposes of this section, it does not matter whether, at the time of receipt of the information or demand:
(a) the person has possession or control of the therapeutic goods to which the information or demand relates; or
(b) the therapeutic goods are in existence.
42U Meaning of actual or potential tampering etc.
Actual or potential tampering, in relation to therapeutic goods, means:
(a) tampering with the therapeutic goods; or
(b) causing the therapeutic goods to be tampered with; or
(c) proposing to tamper with the therapeutic goods; or
(d) proposing to cause the therapeutic goods to be tampered with.
42V Recall of therapeutic goods because of actual or potential tampering
(1) The Secretary may, in writing, impose requirements under this section on a person if:
(a) the person supplies or has supplied therapeutic goods of a particular kind, or a particular batch of therapeutic goods of that kind; and
(b) the Secretary is satisfied that therapeutic goods of that kind, or included in that batch, are, have been or could possibly be, subject to actual or potential tampering.
(2) The requirements may be one or more of the following:
(a) to take specified steps, in the specified manner and within such reasonable period as is specified, to recall therapeutic goods of that kind, or included in that batch, that the person has supplied;
(b) to inform the public or a specified class of persons, in the specified manner and within such reasonable period as is specified, that therapeutic goods of that kind, or included in that batch, are, or have been, subject to actual or potential tampering;
(c) to inform the public or a specified class of persons, in the specified manner and within such reasonable period as is specified, that therapeutic goods of that kind, or included in that batch, could possibly be subject to actual or potential tampering.
(3) Requirements referred to in paragraph (2)(a) do not apply to therapeutic goods that cannot be recalled because they have been administered to, or applied in the treatment of, a person.
(4) The Secretary must cause to be published in the Gazette or on the Department’s website, as soon as practicable after imposing such requirements, a notice setting out particulars of the requirements.
(5) The Secretary may impose requirements under this section whether or not the Secretary has been notified under section 42T.
(6) A person commits an offence if:
(a) the person fails to comply with a requirement under subsection (1) in relation to a supply of therapeutic goods; and
(b) either:
(i) the use of the goods has resulted in, will result in, or is likely to result in, harm or injury to any person; or
(ii) the use of the goods, if the goods were used, would result in, or would be likely to result in, harm or injury to any person; and
(c) the harm or injury has resulted, will result, is likely to result, would result, or would be likely to result, because the person failed to comply with the requirement.
Penalty: Imprisonment for 5 years or 4,000 penalty units, or both.
Note 1: A jury may acquit a person of an offence against this subsection and may convict the person of an offence against subsection (6C) instead: see section 53A.
Note 2: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(6C) A person commits an offence if the person fails to comply with a requirement under subsection (1) in relation to a supply of therapeutic goods.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
(6D) A person commits an offence if the person fails to comply with a requirement under subsection (1) in relation to a supply of therapeutic goods.
Penalty: 100 penalty units.
(6E) An offence against subsection (6D) is an offence of strict liability.
(7) This section does not prevent the Secretary from taking action under section 29D or 30, Division 6 or 7 of Part 3‑2A or Division 1 or 2 of Part 4‑6.
42VA Civil penalty relating to the recall of therapeutic goods because of actual or potential tampering
A person contravenes this section if the person fails to comply with a requirement under subsection 42V(1) in relation to a supply of therapeutic goods.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
42VB Relief from liability for contraventions relating to the recall of therapeutic goods because of actual or potential tampering
(1) If:
(a) proceedings for the contravention of section 42VA (a civil penalty provision) are brought against a person; and
(b) in the proceedings it appears to the Court that the person has, or may have, contravened that section but that:
(i) the person has acted honestly; and
(ii) having regard to all the circumstances of the case, the person ought fairly to be excused for the contravention;
the Court may relieve the person either wholly or partly from a liability to which the person would otherwise be subject, or that might otherwise be imposed on the person, because of the contravention.
(2) If a person thinks that proceedings for the contravention of section 42VA will or may be begun against them, they may apply to the Court for relief.
(3) On an application under subsection (2), the Court may grant relief under subsection (1) as if proceedings had been begun in the Court.
(4) For the purposes of subsection (2) as applying for the purposes of a case tried by a judge with a jury:
(a) a reference in that subsection to the Court is a reference to the judge; and
(b) the relief that may be granted includes withdrawing the case in whole or in part from the jury and directing judgment to be entered for the person on such terms as to costs as the judge thinks appropriate.
42W Supply etc. of therapeutic goods that are subject to recall requirements
(1) A person commits an offence if:
(a) the person supplies therapeutic goods in Australia; and
(b) either:
(i) the person knows that the therapeutic goods are of a kind, or are included in a batch, in respect of which requirements have been imposed under section 42V, on that person or another person, to recall therapeutic goods; or
(ii) the therapeutic goods are of such a kind, or are included in such a batch, and the person is reckless as to that fact; and
(c) the Secretary has not consented in writing to the supply.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) A person commits an offence if:
(a) the person exports therapeutic goods from Australia; and
(b) either:
(i) the person knows that the therapeutic goods are of a kind, or are included in a batch, in respect of which requirements have been imposed under section 42V, on that person or another person, to recall therapeutic goods; or
(ii) the therapeutic goods are of such a kind, or are included in such a batch, and the person is reckless as to that fact; and
(c) the Secretary has not consented in writing to the exportation.
Penalty: Imprisonment for 12 months or 1,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(3) The Secretary must not give consent relating to an exportation unless satisfied that there are exceptional circumstances that justify giving the consent.
42X Saving of other laws
This Part is not intended to exclude or limit the operation of any other law of the Commonwealth or any law of a State or Territory.
Chapter 5A—Enforcement
Part 5A‑1—Civil penalties
Division 1—Obtaining an order for a civil penalty
42Y Federal Court may order person to pay pecuniary penalty for contravening civil penalty provision
Application for order
(1) Within 6 years of a person (the wrongdoer) contravening a civil penalty provision, the Secretary may apply on behalf of the Commonwealth to the Federal Court for an order that the wrongdoer pay the Commonwealth a pecuniary penalty.
Court may order wrongdoer to pay pecuniary penalty
(2) If the Court is satisfied that the wrongdoer has contravened a civil penalty provision, the Court may order the wrongdoer to pay to the Commonwealth for each contravention the pecuniary penalty that the Court determines is appropriate (but not more than the maximum amount specified for the provision).
Determining amount of pecuniary penalty
(3) In determining the pecuniary penalty, the Court must have regard to all relevant matters, including:
(a) the nature and extent of the contravention; and
(b) the nature and extent of any loss or damage suffered as a result of the contravention; and
(c) the circumstances in which the contravention took place; and
(d) whether the person has previously been found by the Court in proceedings under this Act to have engaged in any similar conduct.
Civil evidence and procedure rules apply
(4) The Court must apply the rules of evidence and procedure for civil matters when hearing and determining an application for an order under this section.
Note: The standard of proof in civil proceedings is the balance of probabilities: see section 140 of the Evidence Act 1995.
Conduct contravening more than one civil penalty provision
(5) If conduct constitutes a contravention of 2 or more civil penalty provisions, proceedings may be instituted under this Act against a person in relation to the contravention of any one or more of those provisions. However, the person is not liable to more than one pecuniary penalty under this section in respect of the same conduct.
42YA What is a civil penalty provision?
A subsection of this Act (or a section of this Act that is not divided into subsections) is a civil penalty provision if the words “civil penalty” and one or more amounts in penalty units are set out at the foot of the subsection (or section).
42YC Persons involved in contravening civil penalty provision
(1) A person must not:
(a) aid, abet, counsel or procure a contravention of a civil penalty provision; or
(b) induce (by threats, promises or otherwise) a contravention of a civil penalty provision; or
(c) conspire to contravene a civil penalty provision.
(2) This Act applies to a person who contravenes subsection (1) in relation to a civil penalty provision as if the person had contravened the civil penalty provision.
42YCA Continuing contraventions of civil penalty provisions
(1) If an act or thing is required under a civil penalty provision to be done:
(a) within a particular period; or
(b) before a particular time;
then the obligation to do that act or thing continues until the act or thing is done (even if the period has expired or the time has passed).
(2) A person who contravenes a civil penalty provision that requires an act or thing to be done:
(a) within a particular period; or
(b) before a particular time;
commits a separate contravention of that provision in respect of each day during which the contravention occurs (including the day the order under subsection 42Y(2) is made or any later day).
42YD Recovery of a pecuniary penalty
If the Federal Court orders a person to pay a pecuniary penalty:
(a) the penalty is payable to the Commonwealth; and
(b) the Commonwealth may enforce the order as if it were a judgment of the Court.
42YE Gathering information for application for pecuniary penalty
(1) This section applies if it appears to the Secretary that a person (the wrongdoer) may have contravened a civil penalty provision.
(2) If the Secretary, on reasonable grounds, suspects that a person other than the wrongdoer can give information relevant to an application for a civil penalty order in relation to the contravention, whether or not such an application has been made, the Secretary may, by writing given to the person, require the person to give all reasonable assistance in connection with such an application.
(3) Subsection (2) does not apply in relation to a duly qualified legal practitioner who is acting, or has acted, for the wrongdoer.
(4) If a person fails to give assistance as required under subsection (2), the Federal Court may, on the application of the Secretary, order the person to comply with the requirement as specified in the order.
(5) If a person fails to give assistance as required under subsection (2), the person commits an offence against this subsection.
Penalty: 30 penalty units.
Division 2—Civil penalty proceedings and criminal proceedings
42YF Civil proceedings after criminal proceedings
The Federal Court must not make a pecuniary penalty order against a person for a contravention of a civil penalty provision if the person has been convicted of an offence constituted by conduct that is substantially the same as the conduct constituting the contravention.
42YG Criminal proceedings during civil proceedings
(1) Proceedings for a pecuniary penalty order against a person for a contravention of a civil penalty provision are stayed if:
(a) criminal proceedings are started or have already been started against the person for an offence; and
(b) the offence is constituted by conduct that is substantially the same as the conduct alleged to constitute the contravention.
(2) The proceedings for the order may be resumed if the person is not convicted of the offence. Otherwise, the proceedings for the order are dismissed.
42YH Criminal proceedings after civil proceedings
Criminal proceedings may not be started against a person for conduct that is substantially the same as conduct constituting a contravention of a civil penalty provision if a pecuniary penalty order has been made against the person in respect of that conduct.
42YI Evidence given in proceedings for civil penalty not admissible in criminal proceedings
Evidence of information given or evidence of production of documents by an individual is not admissible in criminal proceedings against the individual if:
(a) the individual previously gave the evidence or produced the documents in proceedings for a pecuniary penalty order against the individual for a contravention of a civil penalty provision (whether or not the order was made); and
(b) the conduct alleged to constitute the offence is substantially the same as the conduct that was claimed to constitute the contravention.
However, this does not apply to a criminal proceeding in respect of the falsity of the evidence given by the individual in the proceedings for the pecuniary penalty order.
Part 5A‑2—Infringement notices
42YJ Simplified outline of this Part
The Secretary can give a person an infringement notice for a contravention of a provision of this Act or the regulations that is an offence of strict liability or for a contravention of a civil penalty provision.
The person can choose to pay an amount as an alternative to having court proceedings brought against the person for the contravention. If the person does not choose to pay the amount, proceedings can be brought against the person in relation to the contravention.
42YK When an infringement notice may be given
(1) If the Secretary reasonably believes that a person has contravened:
(a) a provision of this Act or the regulations that is an offence of strict liability; or
(b) a civil penalty provision;
the Secretary may give to the person an infringement notice for the alleged contravention.
(2) The infringement notice must be given within 12 months after the day on which the contravention is alleged to have taken place.
(3) A single infringement notice must relate only to a single contravention of a single provision unless subsection (4) applies.
(4) The Secretary may give a person a single infringement notice relating to multiple contraventions of a single provision if:
(a) the provision requires the person to do a thing within a particular period or before a particular time; and
(b) the person fails or refuses to do that thing within that period or before that time; and
(c) the failure or refusal occurs on more than 1 day; and
(d) each contravention is constituted by the failure or refusal on one of those days.
Note: For continuing offences, see subsection 4K(2) of the Crimes Act 1914. For continuing contraventions of civil penalty provisions, see section 42YCA of this Act.
42YKA Matters to be included in an infringement notice
(1) An infringement notice must:
(a) be identified by a unique number; and
(b) state the day on which it is given; and
(c) state the name of the person to whom the notice is given; and
(d) state the name and contact details of the person who gave the notice; and
(e) give brief details of the alleged contravention, or each alleged contravention, to which the notice relates, including:
(i) the provision that was allegedly contravened; and
(ii) the maximum penalty that a court could impose for each contravention, if the provision were contravened; and
(iii) the time (if known) and day of, and the place of, each alleged contravention; and
(f) state the amount that is payable under the notice; and
(g) give an explanation of how payment of the amount is to be made; and
(h) state that, if the person to whom the notice is given pays the amount within 28 days after the day the notice is given, then (unless the notice is withdrawn):
(i) if the provision is an offence of strict liability—the person will not be liable to be prosecuted in a court for the alleged contravention; or
(ii) if the provision is a civil penalty provision—proceedings seeking an order under subsection 42Y(2) will not be brought in relation to the alleged contravention; and
(i) state that payment of the amount is not an admission of guilt or liability; and
(j) state that the person may apply to the Secretary to have the period in which to pay the amount extended; and
(k) state that the person may choose not to pay the amount and, if the person does so:
(i) if the provision is an offence of strict liability—the person may be prosecuted in a court for the alleged contravention; or
(ii) if the provision is a civil penalty provision—proceedings seeking an order under subsection 42Y(2) may be brought in relation to the alleged contravention; and
(l) set out how the notice can be withdrawn; and
(m) state that if the notice is withdrawn:
(i) if the provision is an offence of strict liability—the person may be prosecuted in a court for the alleged contravention; or
(ii) if the provision is a civil penalty provision—proceedings seeking an order under subsection 42Y(2) may be brought in relation to the alleged contravention; and
(n) state that the person may make written representations to the Secretary seeking the withdrawal of the notice.
(2) If the notice relates to only one alleged contravention of the provision by the person, the amount to be stated in the notice for the purposes of paragraph (1)(f) is the lesser of:
(a) one‑fifth of the maximum penalty that a court could impose on the person for that contravention; and
(b) 12 penalty units where the person is an individual, or 60 penalty units where the person is a body corporate.
(3) If the notice relates to more than one alleged contravention of the provision by the person, the amount to be stated in the notice for the purposes of paragraph (1)(f) is the lesser of:
(a) one‑fifth of the amount worked out by adding together the maximum penalty that a court could impose on the person for each alleged contravention; and
(b) either:
(i) if the person is an individual—the number of penalty units worked out by multiplying the number of alleged contraventions by 12; or
(ii) if the person is a body corporate—the number of penalty units worked out by multiplying the number of alleged contraventions by 60.
Note: Under section 42YK, a single infringement notice may only deal with multiple contraventions if they are contraventions of a single provision continuing over a period.
42YKB Extension of time to pay amount
(1) A person to whom an infringement notice has been given may apply to the Secretary for an extension of the period referred to in paragraph 42YKA(1)(h).
(2) If the application is made before the end of that period, the Secretary may, in writing, extend that period. The Secretary may do so before or after the end of that period.
(3) If the Secretary extends that period, a reference in this Part, or in a notice or other instrument under this Part, to the period referred to in paragraph 42YKA(1)(h) is taken to be a reference to that period so extended.
(4) If the Secretary does not extend that period, a reference in this Part, or in a notice or other instrument under this Part, to the period referred to in paragraph 42YKA(1)(h) is taken to be a reference to the period that ends on the later of the following days:
(a) the day that is the last day of the period referred to in paragraph 42YKA(1)(h);
(b) the day that is 7 days after the day the person was given notice of the Secretary’s decision not to extend.
(5) The Secretary may extend the period more than once under subsection (2).
42YKC Withdrawal of an infringement notice
Representations seeking withdrawal of notice
(1) A person to whom an infringement notice has been given may make written representations to the Secretary seeking the withdrawal of the notice.
Withdrawal of notice
(2) The Secretary may withdraw an infringement notice given to a person (whether or not the person has made written representations seeking the withdrawal).
(3) When deciding whether or not to withdraw an infringement notice (the relevant infringement notice), the Secretary:
(a) must take into account any written representations seeking the withdrawal that were given by the person to the Secretary; and
(b) may take into account the following:
(i) whether a court has previously imposed a penalty on the person for a contravention of a provision of this Act or the regulations that is an offence of strict liability or for a contravention of a civil penalty provision;
(ii) the circumstances of the alleged contravention;
(iii) whether the person has paid an amount, stated in an earlier infringement notice, for a contravention of a provision of this Act or the regulations that is an offence of strict liability or for a contravention of a civil penalty provision if the contravention is constituted by conduct that is the same, or substantially the same, as the conduct alleged to constitute the contravention in the relevant infringement notice;
(iv) any other matter the Secretary considers relevant.
Notice of withdrawal
(4) Notice of the withdrawal of the infringement notice must be given to the person. The withdrawal notice must state:
(a) the person’s name and address; and
(b) the day the infringement notice was given; and
(c) the identifying number of the infringement notice; and
(d) that the infringement notice is withdrawn; and
(e) that:
(i) if the provision is an offence of strict liability—the person may be prosecuted in a court for the alleged contravention; or
(ii) if the provision is a civil penalty provision—proceedings seeking an order under subsection 42Y(2) may be brought in relation to the alleged contravention.
Refund of amount if infringement notice withdrawn
(5) If:
(a) the Secretary withdraws the infringement notice; and
(b) the person has already paid the amount stated in the notice;
the Commonwealth must refund to the person an amount equal to the amount paid.
42YKD Effect of payment of amount
(1) If the person to whom an infringement notice for an alleged contravention of a provision is given pays the amount stated in the notice before the end of the period referred to in paragraph 42YKA(1)(h):
(a) any liability of the person for the alleged contravention is discharged; and
(b) if the provision is an offence of strict liability—the person may not be prosecuted in a court for the alleged contravention; and
(c) if the provision is a civil penalty provision—proceedings seeking an order under subsection 42Y(2) may not be brought in relation to the alleged contravention; and
(d) the person is not regarded as having admitted guilt or liability for the alleged contravention; and
(e) if the provision is an offence of strict liability—the person is not regarded as having been convicted of the alleged offence.
(2) Subsection (1) does not apply if the notice has been withdrawn.
42YKE Effect of this Part
This Part does not:
(a) require an infringement notice to be given to a person for an alleged contravention of a provision of this Act or the regulations that is an offence of strict liability or an alleged contravention of a civil penalty provision; or
(b) affect the liability of a person for an alleged contravention of a provision of this Act or the regulations that is an offence of strict liability or an alleged contravention of a civil penalty provision if:
(i) the person does not comply with an infringement notice given to the person for the contravention; or
(ii) an infringement notice is not given to the person for the contravention; or
(iii) an infringement notice is given to the person for the contravention and is subsequently withdrawn; or
(c) prevent the giving of 2 or more infringement notices to a person for an alleged contravention of a provision of this Act or the regulations that is an offence of strict liability or an alleged contravention of a civil penalty provision; or
(d) limit a court’s discretion to determine the amount of a penalty to be imposed on a person who is found to have contravened a provision of this Act or the regulations that is an offence of strict liability or to have contravened a civil penalty provision.
Part 5A‑3—Enforceable undertakings
42YL Enforcement of undertakings
(1) The Secretary may accept a written undertaking given by a person in connection with a matter in relation to which the Secretary has a power or function under this Act or the regulations.
(2) The person may withdraw or vary the undertaking at any time, but only with the consent of the Secretary.
(3) The Secretary must publish details of the undertaking, as in force from time to time, on the internet.
(4) If the Secretary considers that the person who gave the undertaking has breached any of its terms, the Secretary may apply to the Federal Court for an order under subsection (5).
(5) If the Court is satisfied that the person has breached a term of the undertaking, the Court may make all or any of the following orders:
(a) an order directing the person to comply with that term of the undertaking;
(b) an order directing the person to pay to the Commonwealth an amount up to the amount of any financial benefit that the person has obtained directly or indirectly and that is reasonably attributable to the breach;
(c) any order that the Court considers appropriate directing the person to compensate any other person who has suffered loss or damage as a result of the breach;
(d) any other order that the Court considers appropriate.
Part 5A‑4—Injunctions
42YM Simplified outline of this Part
The Secretary can seek injunctions from the Federal Court or Federal Circuit Court to restrain a person from contravening this Act or the regulations, or to compel compliance with this Act or the regulations.
Interim injunctions are also available.
42YN Grant of injunctions
Restraining injunctions
(1) If a person has engaged, is engaging or is proposing to engage, in conduct in contravention of this Act or the regulations, the Federal Court or Federal Circuit Court may, on application by the Secretary, grant an injunction:
(a) restraining the person from engaging in the conduct; and
(b) if, in the court’s opinion, it is desirable to do so—requiring the person to do a thing.
Performance injunctions
(2) If:
(a) a person has refused or failed, or is refusing or failing, or is proposing to refuse or fail, to do a thing; and
(b) the refusal or failure was, is or would be a contravention of this Act or the regulations;
the Federal Court or Federal Circuit Court may, on application by the Secretary, grant an injunction requiring the person to do that thing.
42YO Interim injunctions
Grant of interim injunctions
(1) Before deciding an application for an injunction under section 42YN, the Federal Court or Federal Circuit Court may grant an interim injunction:
(a) restraining a person from engaging in conduct; or
(b) requiring a person to do a thing.
No undertakings as to damages
(2) The Federal Court or Federal Circuit Court must not require the Secretary to give an undertaking as to damages as a condition of granting an interim injunction.
42YP Discharging or varying injunctions
The Federal Court or Federal Circuit Court may discharge or vary an injunction granted by that court under this Part.
42YQ Certain limits on granting injunctions not to apply
Restraining injunctions
(1) The power of the Federal Court or Federal Circuit Court under this Part to grant an injunction restraining a person from engaging in conduct may be exercised:
(a) whether or not it appears to the court that the person intends to engage again, or to continue to engage, in conduct of that kind; and
(b) whether or not the person has previously engaged in conduct of that kind; and
(c) whether or not there is an imminent danger of substantial damage to any other person if the person engages in conduct of that kind.
Performance injunctions
(2) The power of the Federal Court or Federal Circuit Court under this Part to grant an injunction requiring a person to do a thing may be exercised:
(a) whether or not it appears to the court that the person intends to refuse or fail again, or to continue to refuse or fail, to do that thing; and
(b) whether or not the person has previously refused or failed to do that thing; and
(c) whether or not there is an imminent danger of substantial damage to any other person if the person refuses or fails to do that thing.
42YR Other powers of court unaffected
The powers conferred on the Federal Court or Federal Circuit Court under this Part are in addition to, and not instead of, any other powers of the court, whether conferred by this Act or otherwise.
Chapter 6—Administration
Part 6‑1—Payment of charges
43 By whom charges payable
(1) An annual registration charge, annual listing charge or annual charge for inclusion in the Register is payable by the person in relation to whom the therapeutic goods concerned are registered, listed or included in the Register.
(2) An annual licensing charge is payable by the holder of the licence to which the charge relates.
(3) An annual conformity assessment body determination charge is payable by the Australian corporation that is the subject of the conformity assessment body determination to which the charge relates.
44 Time for payment of charges
Annual registration charge, annual listing charge or annual charge for inclusion in the Register
(1) An annual registration charge, annual listing charge or annual charge for inclusion in the Register for a financial year becomes payable:
(a) if the registration, listing or inclusion in the Register of the therapeutic goods concerned commenced in that financial year—on the day worked out under the regulations; and
(b) in any other case:
(i) on 1 October in that year; or
(ii) if the regulations specify another day for the purposes of this subparagraph—on that other day in that year.
This subsection is subject to subsection (3).
Annual licensing charge
(2) An annual licensing charge for a financial year becomes payable:
(a) if the licence commenced in that financial year—on the day of that commencement; and
(b) in any other case:
(i) on 1 October in that year; or
(ii) if the regulations specify another day for the purposes of this subparagraph—on that other day in that year.
This subsection is subject to subsection (3).
Annual conformity assessment body determination charge
(2A) An annual conformity assessment body determination charge for a financial year becomes payable:
(a) if the conformity assessment body determination was made in that financial year—on the 28th day after the determination came into force; and
(b) in any other case:
(i) on 1 October in that year; or
(ii) if the regulations specify another day for the purposes of this subparagraph—on that other day in that year.
This subsection is subject to subsection (3).
Charge may become payable on a later day
(3) The Secretary may, by notice in writing given to a person, specify a later day on which a charge referred to in subsection (1), (2) or (2A) becomes payable by the person for a financial year. The notice has effect accordingly.
Interpretation
(4) This section is subject to section 44A.
44A Exemptions from liability to pay charges
(1) The regulations may make provision for and in relation to:
(a) exempting a person from liability to pay annual registration charge, annual listing charge or annual charge for inclusion in the Register for a financial year (the current year) if the person’s turnover of the therapeutic goods concerned for the financial year specified in the regulations is of low value; and
(b) the making of an application for an exemption and requiring payment of that charge for the current year if the application is refused; and
(c) cancelling an exemption and requiring payment of that charge for the current year.
Fees
(2) The regulations may require applications for exemptions to be accompanied by a specified fee. A fee must not be such as to amount to taxation.
Statements prepared by approved persons
(3) The regulations may require a person who is applying for an exemption, or who has been granted an exemption, to provide a statement:
(a) that is prepared by an approved person; and
(b) that specifies whether the person’s turnover of the therapeutic goods concerned for the financial year concerned is of low value.
Additional information
(4) The regulations may provide for the obtaining of additional information or documents from applicants for exemptions or persons granted exemptions.
Merits review
(5) The regulations may provide for review by the Administrative Appeals Tribunal of decisions of the Secretary to refuse applications for exemptions or to cancel exemptions.
No limit on subsection (1)
(6) Subsections (2) to (5) do not limit subsection (1).
Low value turnover
(7) For the purposes of this section, the regulations may specify when a person’s turnover of therapeutic goods for a financial year is of low value. The regulations may specify different rules for different therapeutic goods.
Interpretation
(8) This section does not limit paragraph 63(3)(b) (about the refund, reduction or waiving of fees or charges).
Definitions
(9) In this section:
approved person means a person included in a class of persons specified in regulations made for the purposes of this definition.
turnover has the meaning prescribed by the regulations.
44B Recovery of unpaid charges
An amount of an annual registration charge, an annual listing charge, an annual charge for inclusion in the Register, an annual licensing charge or an annual conformity assessment body determination charge that remains unpaid at the end of the period of 28 days after the day on which the charge becomes payable may be recovered by the Commonwealth as a debt due to the Commonwealth.
Note: Section 44 sets out the day on which a charge becomes payable.
45 Therapeutic Goods Administration Account
(1) There is continued in existence the Therapeutic Goods Administration Account.
Note: The Account was established by subsection 5(3) of the Financial Management Legislation Amendment Act 1999.
(2) The Account is a special account for the purposes of the Public Governance, Performance and Accountability Act 2013.
(3) There must be credited to the Account amounts equal to:
(a) amounts received by the Commonwealth by way of annual registration charge, annual listing charge, annual charge for inclusion in the Register, annual licensing charge and annual conformity assessment body determination charge; and
(b) interest received by the Commonwealth from the investment of an amount standing to the credit of the Account; and
(c) money received by the Commonwealth in relation to property paid for after a debit from the Account; and
(d) money received by the Commonwealth for services provided or to be provided, by or on behalf of the Commonwealth, using amounts standing to the credit of the Account (including amounts received by way of fees payable under the regulations); and
(e) donations for the furtherance of a purpose of the Account that are received by the Commonwealth; and
(f) receipts relating to the recovery of debts (other than debts in respect of statutory fines and penalties) by the Commonwealth that are associated with expenditure of an amount standing to the credit of the Account.
Note: An Appropriation Act provides for amounts to be credited to a special account if any of the purposes of the special account is a purpose that is covered by an item in the Appropriation Act.
(4) The purposes of the Account are to make payments:
(a) to further the objects of this Act (as set out in section 4); and
(b) to enable the Commonwealth to participate in the international harmonisation of regulatory controls on therapeutic goods and other related activities.
Part 6‑2—Entry, searches and warrants
45A Definitions
In this Part, unless the contrary intention appears:
evidential material means:
(a) in respect of an offence against this Act:
(i) any thing with respect to which the offence has been committed or is suspected, on reasonable grounds, to have been committed; or
(ii) any thing as to which there are reasonable grounds for suspecting that it will afford evidence as to the commission of the offence; or
(iii) any thing as to which there are reasonable grounds for suspecting that it is intended to be used for the purpose of committing the offence; and
(b) in respect of a contravention of a civil penalty provision:
(i) any thing with respect to which the civil penalty provision has been contravened or is suspected, on reasonable grounds, of having been contravened; or
(ii) any thing as to which there are reasonable grounds for suspecting that it will afford evidence as to the contravention of the civil penalty provision; or
(iii) any thing as to which there are reasonable grounds for suspecting that it is intended to be used for the purpose of contravening the civil penalty provision.
occupier, in relation to premises, includes a person present at the premises who is in apparent control of the premises.
seize includes secure against interference.
thing includes a substance, and a thing in electronic or magnetic form.
46 Searches to monitor compliance with Act or regulations
(1) Subject to subsections (2) and (3), an authorised person may, for the purpose of finding out whether this Act or the regulations have been complied with:
(a) enter any premises; and
(b) exercise the powers set out in subsection 48(1) and section 48BA.
(2) The authorised person must not enter the premises unless:
(a) the occupier of the premises has consented to the entry; or
(b) the entry is made under a warrant issued under section 49.
(3) An authorised person is not entitled to exercise any powers under subsection (1) in relation to premises if:
(a) the occupier of the premises has required the authorised person to produce his or her identity card for inspection by the occupier; and
(b) the authorised person fails to comply with the requirement.
46A Searches of certain premises to monitor compliance with Act
(1) An authorised person may, subject to subsections (2) and (3), and to the extent that it is reasonably necessary for the purpose of finding out whether this Act or the regulations have been complied with, enter premises to which this section applies and do any of the following:
(a) search the premises and any thing on the premises;
(aa) examine or observe any activity conducted on the premises;
(b) inspect, examine, take measurements of, conduct tests on or take samples of any therapeutic goods on the premises or any thing on the premises that relates to any therapeutic goods;
(c) make any still or moving image or any recording of the premises or any thing on the premises;
(d) inspect any book, record or document on the premises;
(e) take extracts from or make copies of any such book, record or document.
(2) An authorised person must not, under subsection (1), enter premises that are a residence unless:
(a) the occupier of the premises has consented to the entry; or
(b) the premises are used for commercial purposes in relation to therapeutic goods, in addition to residential purposes.
(3) An authorised person is not entitled to exercise any powers under subsection (1) in relation to premises if:
(a) the occupier of the premises has required the authorised person to produce his or her identity card for inspection by the occupier; and
(b) the authorised person fails to comply with the requirement.
(4) This section applies to:
(a) premises of a person:
(ia) who is required to comply with a condition of an exemption of therapeutic goods under section 18A; or
(i) who has been granted an approval or authority under subsection 19(1) or (5); or
(ii) who has been granted an approval under section 19A; or
(iiaaa) who is required to comply with a condition of an exemption of biologicals under section 32CB; or
(iiaab) who has been granted an approval under subsection 32CK(1) or an authority under subsection 32CM(1); or
(iiaac) who has been granted an approval under subsection 32CO(1), (1A) or (2); or
(iiaa) who is required to comply with a condition of an exemption of a kind of medical device under section 41GS; or
(iia) who has been granted an approval or authority under subsection 41HB(1) or 41HC(1); or
(iib) who has been granted an approval under subsection 41HD(1), (1A) or (2); or
(iii) in relation to whom therapeutic goods are registered, listed or included in the Register;
being premises connected with:
(iv) the importation, export, manufacture or supply of therapeutic goods; or
(v) the keeping of documents relating to the importation, export, manufacture or supply of therapeutic goods; or
(vi) the keeping of records in compliance with a condition under paragraph 28(5)(c) or (ca) or 32EC(2)(c); and
(b) premises to which the person in relation to whom therapeutic goods are registered, listed or included in the Register, or the sponsor of the goods, must allow access as a condition of the registration, listing or inclusion; and
(c) premises in relation to which a licence has been granted under Part 3‑3 for, or a conformity assessment certificate issued under Part 4‑4, in relation to the manufacture of therapeutic goods, or premises at which records are kept in relation to such manufacture; and
(d) premises of a person who has been issued with, or who has applied for, an Australian conformity assessment body certificate.
46B Searches and seizures on public health grounds
(1) Subject to subsection (2), if an authorised person has reasonable grounds for suspecting that:
(a) there may be on any premises a particular thing in respect of which this Act or the regulations have not been complied with; and
(b) it is necessary in the interests of public health to exercise powers under this section in order to avoid an imminent risk of death, serious illness or serious injury;
the authorised person may, to the extent that it is reasonably necessary for the purpose of avoiding an imminent risk of death, serious illness or serious injury, enter the premises and do any of the following:
(c) search the premises for the thing;
(d) if the authorised person finds the thing on the premises—seize it.
(2) An authorised person is not entitled to exercise any powers under subsection (1) in relation to premises if:
(a) the occupier of the premises has required the authorised person to produce his or her identity card for inspection by the occupier; and
(b) the authorised person fails to comply with the requirement.
47 Searches and seizures related to offences and civil penalty provisions
(1) Subject to subsections (2) and (3), if an authorised person has reasonable grounds for suspecting that there may be evidential material in respect of an offence against this Act, in respect of a contravention of a civil penalty provision or in respect of both on any premises, the authorised person may:
(a) enter the premises; and
(b) exercise the powers set out in subsection (4), subsection 48(1) and section 48C; and
(c) if the authorised person finds the thing on the premises—seize it.
(2) The authorised person must not enter the premises unless:
(a) the occupier of the premises has consented to the entry; or
(b) the entry is made under a warrant issued under section 50.
(3) An authorised person is not entitled to exercise any powers under subsection (1) in relation to premises if:
(a) the occupier of the premises has required the authorised person to produce his or her identity card for inspection by the occupier; and
(b) the authorised person fails to comply with the requirement.
(4) If:
(a) in the course of searching, in accordance with a warrant, for a particular thing, an authorised person finds another thing that the authorised person believes on reasonable grounds to be evidential material in respect of an offence against this Act, in respect of a contravention of a civil penalty provision or in respect of both; and
(b) the authorised person believes, on reasonable grounds, that it is necessary to seize that other thing in order to prevent its concealment, loss or destruction, or its use:
(i) in committing, continuing or repeating an offence against this Act; or
(ii) in committing, continuing or repeating a contravention of a civil penalty provision;
the warrant is taken to authorise the authorised person to seize that other thing.
48 General powers of authorised persons in relation to premises
(1) The powers an authorised person may exercise under paragraphs 46(1)(b) and 47(1)(b) are as follows:
(a) to search the premises and any thing on the premises;
(aa) to examine or observe any activity conducted on the premises;
(b) to inspect, examine, take measurements of, conduct tests on or take samples of any therapeutic goods on the premises or any thing on the premises that relates to any therapeutic goods;
(c) to make any still or moving image or any recording of the premises or any thing on the premises;
(d) if the authorised person was only authorised to enter the premises because the occupier of the premises consented to the entry—to require the occupier to:
(i) answer any questions put by the authorised person; and
(ii) produce any book, record or document requested by the authorised person;
(e) if the authorised person was authorised to enter the premises by a warrant under section 49 or 50—to require any person in or on the premises to:
(i) answer any questions put by the authorised person; and
(ii) produce any book, record or document requested by the authorised person;
(f) to inspect any book, record or document on the premises;
(g) to take extracts from or make copies of any such book, record or document;
(h) to take onto the premises such equipment and materials as the authorised person requires for the purpose of exercising powers in relation to the premises.
(3) A person must not refuse or fail to comply with a requirement under paragraph (1)(e).
Penalty: 30 penalty units.
(3A) Subsection (3) does not apply if the person has a reasonable excuse.
Note: The defendant bears an evidential burden in relation to the matter in subsection (3A). See subsection 13.3(3) of the Criminal Code.
(4) It is a reasonable excuse for a person to refuse or fail to answer a question or produce a document if answering the question, or producing the document, would tend to incriminate the person.
48A Details of warrant to be given to occupier etc.
(1) If a warrant in relation to premises is being executed and the occupier of the premises or another person who apparently represents the occupier is present at the premises, the authorised person must make available to that person a copy of the warrant.
(2) The authorised person must identify himself or herself to that person.
(3) The copy of the warrant referred to in subsection (1) need not include the signature of the magistrate who issued the warrant.
48AA Completing execution of warrant under section 50 after temporary cessation
(1) This section applies if an authorised person who is executing a warrant under section 50 in relation to premises temporarily ceases its execution and leaves the premises.
(2) The authorised person may complete the execution of the warrant if:
(a) the warrant is still in force; and
(b) the authorised person is absent from the premises:
(i) for not more than 1 hour; or
(ii) if there is an emergency situation, for not more than 12 hours or such longer period as allowed by a magistrate under subsection (5); or
(iii) for a longer period if the occupier of the premises consents in writing.
Application for extension in emergency situation
(3) An authorised person may apply to a magistrate for an extension of the 12‑hour period mentioned in subparagraph (2)(b)(ii) if:
(a) there is an emergency situation; and
(b) the authorised person believes on reasonable grounds that the authorised person will not be able to return to the premises within that period.
(4) If it is practicable to do so, before making the application, the authorised person must give notice to the occupier of the premises of his or her intention to apply for an extension.
Extension in emergency situation
(5) A magistrate may extend the period during which the authorised person may be away from the premises if:
(a) an application is made under subsection (3); and
(b) the magistrate is satisfied, by information on oath or affirmation, that there are exceptional circumstances that justify the extension; and
(c) the extension would not result in the period ending after the warrant ceases to be in force.
48B Announcement before entry
(1) An authorised person must, before entering the premises under a warrant:
(a) announce that he or she is authorised to enter the premises; and
(b) give any person at the premises an opportunity to allow entry to the premises.
(2) An authorised person is not required to comply with subsection (1) if he or she believes on reasonable grounds that immediate entry to the premises is required to ensure:
(a) the safety of a person; or
(b) that the effective execution of the warrant is not frustrated.
48BA Use of electronic equipment at premises for monitoring compliance with Act or regulations
(1) An authorised person may operate electronic equipment at the premises to see whether information relevant to determining whether this Act or the regulations have been complied with is accessible by doing so.
(2) If the authorised person, after operating the equipment, finds that information relevant to determining whether this Act or the regulations have been complied with is accessible by doing so, he or she may:
(a) operate electronic equipment on the premises to put the information in documentary form and remove the documents so produced from the premises; or
(b) operate electronic equipment on the premises to transfer the information to a disk, tape or other storage device that:
(i) is brought to the premises for the exercise of the power; or
(ii) is on the premises and the use of which for that purpose has been agreed in writing by the occupier of the premises;
and remove the disk, tape or other storage device from the premises.
(3) An authorised person may operate electronic equipment as mentioned in subsection (1) or (2) only if the authorised person believes on reasonable grounds that the operation of the equipment can be carried out without damage to the equipment.
Note: For compensation for damage to electronic equipment, see section 48D.
(4) If the authorised person believes on reasonable grounds that:
(a) information relevant to determining whether this Act or the regulations have been complied with may be accessible by operating electronic equipment at the premises; and
(b) expert assistance is required to operate the equipment; and
(c) if he or she does not take action under this subsection, the information may be destroyed, altered or otherwise interfered with;
he or she may do whatever is necessary to secure the equipment, whether by locking it up, placing a guard or otherwise.
(5) The authorised person must give notice to the occupier of the premises of his or her intention to secure equipment and of the fact that the equipment may be secured for up to 24 hours.
(6) The equipment may be secured:
(a) for a period not exceeding 24 hours; or
(b) until the equipment has been operated by the expert;
whichever happens first.
(7) The authorised person may apply to a magistrate for an extension of the 24‑hour period if the authorised person believes on reasonable grounds that the equipment needs to be secured for longer than that period.
(8) The authorised person must give notice to the occupier of the premises of his or her intention to apply for an extension, and the occupier is entitled to be heard in relation to the application.
(9) The 24‑hour period may be extended more than once.
48C Use of electronic equipment at premises relating to offences and civil penalty provisions
(1) An authorised person may operate electronic equipment at the premises to see whether evidential material in respect of an offence against this Act, in respect of a contravention of a civil penalty provision or in respect of both is accessible by doing so.
(2) If the authorised person, after operating the equipment, finds that evidential material in respect of an offence against this Act, in respect of a contravention of a civil penalty provision or in respect of both is accessible by doing so, he or she may:
(a) seize the equipment and any disk, tape or other associated device; or
(b) operate electronic equipment on the premises to put the evidential material in documentary form and remove the documents so produced from the premises; or
(c) operate electronic equipment on the premises to transfer the evidential material to a disk, tape or other storage device that:
(i) is brought to the premises for the exercise of the power; or
(ii) is on the premises and the use of which for that purpose has been agreed in writing by the occupier of the premises;
and remove the disk, tape or other storage device from the premises.
(2A) An authorised person may operate electronic equipment as mentioned in subsection (1) or (2) only if the authorised person believes on reasonable grounds that the operation of the equipment can be carried out without damage to the equipment.
Note: For compensation for damage to electronic equipment, see section 48D.
(3) An authorised person may seize equipment under paragraph (2)(a) only if:
(a) it is not practicable to put the material in documentary form as mentioned in paragraph (2)(b) or to transfer the material as mentioned in paragraph (2)(c); or
(b) possession by the occupier of the equipment could constitute an offence.
(4) If the authorised person believes on reasonable grounds that:
(a) evidential material in respect of an offence against this Act, in respect of a contravention of a civil penalty provision or in respect of both may be accessible by operating electronic equipment at the premises; and
(b) expert assistance is required to operate the equipment; and
(c) if he or she does not take action under this subsection, the material may be destroyed, altered or otherwise interfered with;
he or she may do whatever is necessary to secure the equipment, whether by locking it up, placing a guard or otherwise.
(5) The authorised person must give notice to the occupier of the premises of his or her intention to secure equipment and of the fact that the equipment may be secured for up to 24 hours.
(6) The equipment may be secured:
(a) for a period not exceeding 24 hours; or
(b) until the equipment has been operated by the expert;
whichever happens first.
(7) The authorised person may apply to a magistrate for an extension of the 24‑hour period if the authorised person believes on reasonable grounds that the equipment needs to be secured for longer than that period.
(8) The authorised person must give notice to the occupier of the premises of his or her intention to apply for an extension, and the occupier is entitled to be heard in relation to the application.
(9) The 24‑hour period may be extended more than once.
48D Compensation for damage to electronic equipment
(1) If:
(a) damage is caused to equipment as a result of it being operated as mentioned in section 48BA or 48C; and
(b) the damage was caused as a result of:
(i) insufficient care being exercised in selecting the person who was to operate the equipment; or
(ii) insufficient care being exercised by the person operating the equipment;
compensation for the damage is payable to the owner of the equipment.
(2) Compensation is payable out of money appropriated by the Parliament for the purpose.
(3) In determining the amount of compensation payable, regard is to be had to whether the occupier of the premises and his or her employees and agents, if they were available at the time, had provided any warning or guidance as to the operation of the equipment that was appropriate in the circumstances.
48E Copies of seized things to be provided
(1) Subject to subsection (2), if an authorised person seizes, under a warrant relating to premises:
(a) a document, film, computer file or other thing that can be readily copied; or
(b) a storage device the information in which can be readily copied;
the authorised person must, if requested to do so by the occupier of the premises or another person who apparently represents the occupier and who is present when the warrant is executed, give a copy of the thing or the information to that person as soon as practicable after the seizure.
(2) Subsection (1) does not apply if possession of the document, film, computer file, thing or information by the occupier could constitute an offence against a law of the Commonwealth or contravention of a civil penalty provision.
48F Occupier entitled to be present during search
(1) If a warrant in relation to premises is being executed and the occupier of the premises or another person who apparently represents the occupier is present at the premises, the person is entitled to observe the search being conducted.
(2) The right to observe the search being conducted ceases if the person impedes the search.
(3) This section does not prevent 2 or more areas of the premises being searched at the same time.
48FA Responsibility to provide facilities and assistance
(1) The occupier of premises to which a warrant relates, or another person who apparently represents the occupier, must provide an authorised person executing the warrant with all reasonable facilities and assistance for the effective exercise of the authorised person’s powers.
(2) A person commits an offence if:
(a) the person is subject to subsection (1); and
(b) the person fails to comply with that subsection.
Penalty for contravention of this subsection: 30 penalty units.
48G Receipts for things seized under warrant
(1) If a thing is seized under this Part, the authorised person must provide a receipt for the thing.
(2) If 2 or more things are seized or moved, they may be covered in the one receipt.
48H Retention of seized things
(1) Subject to any contrary order of a court, if an authorised person seizes a thing under this Part, an authorised person must return it if:
(a) the reason for its seizure no longer exists or it is decided that it is not to be used in evidence; or
(b) the period of 90 days after its seizure ends;
whichever first occurs, unless the thing is forfeited or forfeitable to the Commonwealth.
(2) At the end of the 90 days specified in subsection (1), an authorised person must take reasonable steps to return the thing to the person from whom it was seized, unless:
(a) proceedings in respect of which the thing may afford evidence were instituted before the end of the 90 days and have not been completed (including an appeal to a court in relation to those proceedings); or
(b) an authorised person may retain the thing because of an order under section 48J; or
(c) an authorised person is otherwise authorised (by a law, or an order of a court, of the Commonwealth or of a State or Territory) to retain, destroy or dispose of the thing.
(3) The thing may be returned under subsection (2) either unconditionally or on such terms and conditions as the Secretary sees fit.
48J Magistrate may permit a thing to be retained
(1) An authorised person may apply to a magistrate for an order that he or she may retain the thing for a further period if:
(a) before the end of 90 days after the seizure; or
(b) before the end of a period previously specified in an order of a magistrate under this section;
proceedings in respect of which the thing may afford evidence have not commenced.
(2) If the magistrate is satisfied that it is necessary for an authorised person to continue to retain the thing:
(a) for the purposes of an investigation as to whether an offence against this Act has been committed; or
(b) to enable evidence of an offence against this Act to be secured for the purposes of a prosecution; or
(c) for the purposes of an investigation as to whether a civil penalty provision has been contravened; or
(d) to enable evidence of a contravention of a civil penalty provision to be secured for the purposes of civil proceedings;
the magistrate may order that an authorised person may retain the thing for a period (not being a period exceeding 3 years) specified in the order.
(3) Before making the application, the authorised person must:
(a) take reasonable steps to discover who has an interest in the retention of the thing; and
(b) if it is practicable to do so, notify each person whom the authorised person believes to have such an interest of the proposed application.
49 Monitoring warrants
(1) An authorised person may apply to a magistrate for a warrant under this section in relation to premises.
(2) Subject to subsection (3), the magistrate may issue the warrant if the magistrate is satisfied, by information on oath, that it is reasonably necessary that one or more authorised persons should have access to the premises for the purposes of finding out whether this Act or the regulations have been complied with.
(3) The magistrate must not issue the warrant unless the authorised person or some other person has given to the magistrate, either orally or by affidavit, such further information (if any) as the magistrate requires concerning the grounds on which the issue of the warrant is being sought.
(4) The warrant must:
(a) authorise one or more authorised persons (whether or not named in the warrant), with such assistance and by such force as is necessary and reasonable:
(i) to enter the premises; and
(ii) to exercise the powers set out in subsection 48(1) and section 48BA in relation to the premises; and
(b) state whether the entry is authorised to be made at any time of the day or night or during specified hours of the day or night; and
(c) specify the day (not more than 6 months after the issue of the warrant) on which the warrant ceases to have effect; and
(d) state the purpose for which the warrant is issued.
50 Offence and civil penalty provision related warrants
(1) An authorised person may apply to a magistrate for a warrant under this section in relation to premises.
(2) Subject to subsection (3), the magistrate may issue the warrant if the magistrate is satisfied, by information on oath, that there are reasonable grounds for suspecting that there is, or there may be within the next 72 hours, in or on the premises evidential material in respect of an offence against this Act, in respect of a contravention of a civil penalty provision or in respect of both.
(3) The magistrate must not issue the warrant unless the authorised person or some other person has given to the magistrate, either orally or by affidavit, such further information (if any) as the magistrate requires concerning the grounds on which the issue of the warrant is being sought.
(4) The warrant must:
(a) name one or more authorised persons; and
(b) authorise the persons so named, with such assistance and by such force as is necessary and reasonable:
(i) to enter the premises; and
(ii) to exercise the powers set out in subsections 47(4) and 48(1) and section 48C; and
(iii) to seize the evidential material; and
(c) state whether the entry is authorised to be made at any time of the day or night or during specified hours of the day or night; and
(d) specify the day (not more than one week after the issue of the warrant) on which the warrant ceases to have effect; and
(e) state the purpose for which the warrant is issued.
51 Offence and civil penalty provision related warrants by telephone
(1) If, in an urgent case, an authorised person considers it necessary to do so, the person may apply to a magistrate by telephone for a warrant under section 50 in relation to premises.
(2) Before applying for the warrant, the person must prepare an information of the kind mentioned in subsection 50(2) in relation to the premises that sets out the grounds on which the warrant is sought.
(3) If it is necessary to do so, the person may apply for the warrant before the information is sworn.
(4) If the magistrate is satisfied:
(a) after having considered the terms of the information; and
(b) after having received such further information (if any) as the magistrate requires concerning the grounds on which the issue of the warrant is being sought;
that there are reasonable grounds for issuing the warrant, the magistrate may complete and sign the same warrant that the magistrate would issue under section 50 if the application had been made under that section.
(5) If the magistrate completes and signs the warrant:
(a) the magistrate must:
(i) tell the authorised person what the terms of the warrant are; and
(ii) tell the authorised person the day on which and the time at which the warrant was signed; and
(iii) tell the authorised person the day (not more than one week after the magistrate completes and signs the warrant) on which the warrant ceases to have effect; and
(iv) record on the warrant the reasons for granting the warrant; and
(b) the authorised person must:
(i) complete a form of warrant in the same terms as the warrant completed and signed by the magistrate; and
(ii) write on the form the name of the magistrate and the day on which and the time at which the warrant was signed.
(6) The authorised person must also, not later than the day after the day of expiry or execution of the warrant, whichever is the earlier, send to the magistrate:
(a) the form of warrant completed by the person; and
(b) the information referred to in subsection (2), which must have been duly sworn.
(7) When the magistrate receives those documents, the magistrate must:
(a) attach them to the warrant that the magistrate completed and signed; and
(b) deal with them in the way in which the magistrate would have dealt with the information if the application had been made under section 50.
(8) A form of warrant duly completed under subsection (5) is authority for any entry, search, seizure or other exercise of a power that the warrant signed by the magistrate authorises.
(9) If:
(a) it is material, in any proceedings, for a court to be satisfied that an exercise of a power was authorised by this section; and
(b) the warrant signed by the magistrate authorising the exercise of the power is not produced in evidence;
the court must assume, unless the contrary is proved, that the exercise of the power was not authorised by such a warrant.
(10) A reference in this Part to a warrant under section 50 includes a reference to a warrant signed by a magistrate under this section.
51A Inspections for purposes of Mutual Recognition Convention
(1) A person may request the Secretary to arrange for an authorised person to inspect premises, and specified processes being carried out on those premises, for the purposes of paragraph 2 of Article 3 of the Mutual Recognition Convention.
(2) An authorised person may make an inspection in accordance with arrangements under subsection (1).
51B Offences relating to warrants
(1) A person must not make, in an application for a warrant, a statement that the person knows to be false or misleading in a material particular.
Penalty: Imprisonment for 2 years.
(2) A person must not:
(a) state in a document that purports to be a form of warrant under section 51 the name of a magistrate unless that magistrate issued the warrant; or
(b) state on a form of warrant under that section a matter that, to the person’s knowledge, departs in a material particular from the form authorised by the magistrate; or
(c) purport to execute, or present to another person, a document that purports to be a form of warrant under that section that the first‑mentioned person knows:
(i) has not been approved by a magistrate under that section; or
(ii) to depart in a material particular from the terms authorised by a magistrate under that section; or
(d) give to a magistrate a form of warrant under that section that is not the form of warrant that the person purported to execute.
Penalty: Imprisonment for 2 years.
52 Identity cards
(1) The Secretary is to ensure that each authorised person is issued with an identity card that incorporates a recent photograph of the person.
(3) Where a person ceases to be an authorised person, the person must, as soon as practicable after so ceasing, return the person’s identity card to the Secretary.
Penalty: 1 penalty unit.
(4) An offence under subsection (3) is an offence of strict liability.
Note: For strict liability, see section 6.1 of the Criminal Code.
Part 6‑3—Scheduling of substances
52AA Overview
This Part provides the basis for a uniform system in Australia of access controls for goods containing scheduled substances.
The scheduling of substances allows restrictions to be placed on their supply to the public, in the interests of public health and safety. This is aimed at minimising the risks of poisoning from, and the misuse and abuse of, scheduled substances.
52A Definitions
(1) In this Part, unless the contrary intention appears:
current Poisons Standard means:
(a) if no document has been prepared under paragraph 52D(2)(b)—the first Poisons Standard; or
(b) otherwise—the document last prepared under that paragraph (including as amended).
first Poisons Standard means the latest edition at the commencement of this Part of the document known as the Standard for the Uniform Scheduling of Drugs and Poisons published by the Australian Health Ministers’ Advisory Council.
scheduling, in relation to a substance, means determining the schedule or schedules to the current Poisons Standard in which the name or a description of the substance is to be included.
substance means:
(a) an ingredient, compound, material or preparation which, or the use of which, may cause death, illness or injury to persons or animals; or
(b) an ingredient, compound, material or preparation specified under subsection (2);
and includes any ingredient, compound, material or preparation referred to in a schedule to the current Poisons Standard (as in force immediately before 1 July 2010).
(2) The Secretary may, by legislative instrument, specify an ingredient, compound, material or preparation for the purposes of paragraph (b) of the definition of substance in subsection (1).
Note: For specification by class, see subsection 13(3) of the Legislation Act 2003.
52B Advisory Committee on Medicines Scheduling
(1) The Advisory Committee on Medicines Scheduling is established by this section.
(2) Subject to subsection (3), the Committee is to be constituted, and to hold meetings, in accordance with the regulations.
(3) The Commonwealth, each State, the Australian Capital Territory and the Northern Territory are each entitled to nominate a member of the Committee in accordance with the regulations.
(4) The functions of the Committee are as follows:
(a) subject to subsection (5), to make recommendations to the Secretary in relation to the classification and scheduling of substances that are, or are included in, therapeutic goods;
(b) to make recommendations to the Secretary in relation to other changes to the current Poisons Standard (other than the schedules);
(c) to reconsider a recommendation made under paragraph (a) or (b) at the request of the Secretary;
(d) subject to subsection (5), to provide advice to the Secretary in relation to the restrictions (including restrictions as to accessibility and availability) to be imposed in respect of particular substances that are, or are included in, therapeutic goods;
(e) to provide advice to the Secretary in relation to any matter referred to it by the Secretary;
(f) any other functions that are prescribed by the regulations.
(5) Paragraphs (4)(a) and (d) do not apply in relation to substances to the extent that the substances are included in goods other than therapeutic goods.
52C Advisory Committee on Chemicals Scheduling
(1) The Advisory Committee on Chemicals Scheduling is established by this section.
(2) Subject to subsection (3), the Committee is to be constituted, and to hold meetings, in accordance with the regulations.
(3) The Commonwealth, each State, the Australian Capital Territory and the Northern Territory are each entitled to nominate a member of the Committee in accordance with the regulations.
(4) The functions of the Committee are as follows:
(a) subject to subsection (5), to make recommendations to the Secretary in relation to the classification and scheduling of substances;
(b) to make recommendations to the Secretary in relation to other changes to the current Poisons Standard (other than the schedules);
(c) to reconsider a recommendation made under paragraph (a) or (b) at the request of the Secretary;
(d) subject to subsection (5), to provide advice to the Secretary in relation to the restrictions (including restrictions as to accessibility and availability) to be imposed in respect of particular substances;
(e) to provide advice to the Secretary in relation to any matter referred to it by the Secretary;
(f) any other functions that are prescribed by the regulations.
(5) Paragraphs (4)(a) and (d) do not apply in relation to substances to the extent that the substances are, or are included in, therapeutic goods.
52CA Joint meetings
The Advisory Committee on Medicines Scheduling and the Advisory Committee on Chemicals Scheduling may hold joint meetings in accordance with the regulations.
52D Poisons Standard
(1) On the commencement of this Part, the first Poisons Standard is taken to have been prepared and made available by the then National Drugs and Poisons Schedule Committee.
(2) Subject to this Act and the regulations, the Secretary may:
(a) amend the current Poisons Standard; or
(b) prepare a document (including schedules containing the names or descriptions of substances or classes of substances), in substitution for the current Poisons Standard.
(3) The Secretary may exercise a power under subsection (2) on the Secretary’s own initiative or following an application under section 52EAA.
(4A) An instrument made under paragraph (2)(a) or (b) after the commencement of this subsection is a legislative instrument, but section 42 (disallowance) of the Legislation Act 2003 does not apply to the instrument.
(4B) Despite subsection 14(2) of the Legislation Act 2003, an instrument made under paragraph (2)(a) or (b) of this section may make provision in relation to a matter by applying, adopting or incorporating any matter contained in an instrument or other writing as in force or existing from time to time.
(5) In this section:
amend, in relation to the current Poisons Standard, means:
(a) alter any provision (including a reference to a substance) in the current Poisons Standard; or
(b) omit any provision (including a reference to a substance) from the current Poisons Standard; or
(c) insert any provision (including a reference to a substance) in the current Poisons Standard.
52E Secretary to take certain matters into account in exercising powers
(1) In exercising a power under subsection 52D(2), the Secretary must take the following matters into account (where relevant):
(a) the risks and benefits of the use of a substance;
(b) the purposes for which a substance is to be used and the extent of use of a substance;
(c) the toxicity of a substance;
(d) the dosage, formulation, labelling, packaging and presentation of a substance;
(e) the potential for abuse of a substance;
(f) any other matters that the Secretary considers necessary to protect public health.
(2) In exercising a power under subsection 52D(2), the Secretary must comply with any guidelines of:
(a) the Australian Health Ministers’ Advisory Council; and
(b) the subcommittee of the Council known as the National Coordinating Committee on Therapeutic Goods (or any replacement subcommittee);
notified to the Secretary for the purposes of this section.
(3) In exercising a power under subsection 52D(2), the Secretary must have regard to any recommendations or advice of the Advisory Committee on Medicines Scheduling or the Advisory Committee on Chemicals Scheduling.
(4) In exercising a power under subsection 52D(2), the Secretary may seek advice from either or both of the following:
(a) any committee that the Secretary considers appropriate (whether or not the committee is established under this Act or the regulations);
(b) any person.
(5) Subsections (2) to (4) do not limit the information the Secretary may consider in exercising a power under subsection 52D(2).
52EAA Application for amendment of the Poisons Standard
(1) A person may apply to the Secretary for an amendment of the current Poisons Standard.
(2) An application under subsection (1) must:
(a) be made in accordance with a form approved by the Secretary; and
(b) set out the amendment sought; and
(c) be delivered to an office of the Department specified in the form; and
(d) be accompanied by the prescribed application fee.
Further information
(3) The Secretary may, by notice in writing given to the person, require the person to give to the Secretary, within such reasonable time as is specified in the notice, such further information concerning the application as is specified in the notice.
Applications or information may be given electronically
(4) An approval of a form mentioned in paragraph (2)(a), or a notice mentioned in subsection (3), may require or permit an application or information to be given in accordance with specified software requirements:
(a) on a specified kind of data processing device; or
(b) by way of a specified kind of electronic transmission.
52EC Review of scheduling regime
(1) The Minister must cause an independent review of the operation of this Part to be conducted, with particular reference to the amendments to this Part made by the Therapeutic Goods Amendment (2009 Measures No. 2) Act 2009 (the amendments).
(2) The review must:
(a) start not later than 1 July 2013; and
(b) be completed within 6 months.
(3) The review must report on:
(a) the system of access controls for goods containing scheduled substances established by this Part;
(b) the outcomes of the administration of scheduled substances by the Secretary and by the committees established by this Part;
(c) the effect of the amendments on the therapeutic goods industry and on individual parties within the industry;
(d) whether there are adequate avenues for review of decisions made by the Secretary and by the committees established by this Part;
and may make recommendations for further changes to the scheduling regime.
(4) The review must be conducted by a panel which must comprise not less than three, and not more than five, persons with relevant expertise.
(5) As part of the review, the panel must invite and consider public submissions.
(6) The panel must give the Minister a written report of the review.
(7) The Minister must cause a copy of the report to be laid before each House of the Parliament within 15 sitting days of that House after the day on which the Minister receives the report.
Chapter 7—Miscellaneous
53 Retention of material on withdrawal of application
Where a person withdraws an application for:
(a) registration; or
(b) listing; or
(ba) inclusion of a biological in the Register; or
(c) a conformity assessment certificate; or
(d) inclusion of a kind of medical device in the Register; or
(e) a licence;
the Department may retain the application and any material submitted in connection with the application.
53A Alternative verdicts for various offences
If a jury acquits a person of an offence against a provision listed in column 2 of an item in the following table, but is satisfied beyond reasonable doubt of facts that prove that the person is guilty of the offence listed in column 3 of that item, the jury may convict the person of the offence listed in column 3 of that item:
Alternative verdicts for various offences |
Column 1 | Column 2 | Column 3 |
Item | If a prosecution is for an offence against... | the jury may instead convict the person of an offence against... |
1A | subsection 9G(1) | subsection 9G(4) |
1 | subsection 14(1) | subsection 14(4) |
2 | subsection 14(6) | subsection 14(9) |
3 | subsection 14(10) | subsection 14(13) |
4 | subsection 15(2) | subsection 15(5) |
5 | subsection 19B(1) | subsection 19B(4) |
6 | subsection 21A(1) | subsection 21A(4) |
7 | subsection 21A(5) | subsection 21A(8) |
8 | subsection 21A(9) | subsection 21A(9A) |
8A | subsection 21A(11A) | subsection 21A(11C) |
9 | subsection 21A(12) | subsection 21A(12A) |
9A | subsection 22(2) | subsection 22(3) |
10 | subsection 22A(1) | subsection 22A(4) |
11 | subsection 30EC(1) | subsection 30EC(4) |
12 | subsection 30F(4B) | subsection 30F(5) |
13 | subsection 31(5A) | subsection 31(6) |
13A | subsection 32BA(1) | subsection 32BA(4) |
13B | subsection 32BB(1) | subsection 32BB(4) |
13C | subsection 32BC(1) | subsection 32BC(4) |
13D | subsection 32BD(1) | subsection 32BD(4) |
13E | subsection 32BI(1) | subsection 32BI(4) |
13EA | subsection 32BJ(2A) | subsection 32BJ(2B) |
13EB | subsection 32CJ(6) | subsection 32CJ(7) |
13F | subsection 32CN(1) | subsection 32CN(4) |
13FA | subsection 32CN(5) | subsection 32CN(7) |
13G | subsection 32DO(1) | subsection 32DO(4) |
13H | subsection 32EF(1) | subsection 32EF(4) |
13J | subsection 32HC(1) | subsection 32HC(4) |
13K | subsection 32JB(2) | subsection 32JB(5) |
14 | subsection 35(1) | subsection 35(4) |
15 | subsection 35(5) | subsection 35(9) |
16 | subsection 35B(1) | subsection 35B(4) |
17 | subsection 41EI(1) | subsection 41EI(4) |
18 | subsection 41FE(1) | subsection 41FE(4) |
19 | subsection 41JB(4) | subsection 41JB(7) |
20 | subsection 41KC(1) | subsection 41KC(4) |
21 | subsection 41MA(1) | subsection 41MA(4) |
22 | subsection 41MA(5) | subsection 41MA(8) |
23 | subsection 41MA(9) | subsection 41MA(12) |
24 | subsection 41MC(2) | subsection 41MC(5) |
25 | subsection 41ME(1) | subsection 41ME(4) |
26 | subsection 41ME(5) | subsection 41ME(8) |
27 | subsection 41MF(1) | subsection 41MF(2) |
28 | subsection 41MF(3) | subsection 41MF(4) |
29 | subsection 41MI(1) | subsection 41MI(4) |
29A | subsection 41ML(1) | subsection 41ML(2) |
30 | subsection 41MN(1) | subsection 41MN(4) |
31 | subsection 41MN(5) | subsection 41MN(8) |
31A | subsection 41MN(10) | subsection 41MN(11) |
32 | subsection 41MO(1) | subsection 41MO(4) |
32A | subsection 41MO(4A) | subsection 41MO(4C) |
33 | subsection 41MO(5) | subsection 41MO(8) |
33A | subsection 42DL(1) | subsection 42DL(2) |
33B | subsection 42DLA(1) | subsection 42DLA(2) |
33C | subsection 42DM(1) | subsection 42DM(2) |
33D | subsection 42DW(1) | subsection 42DW(2) |
34 | subsection 42V(6) | subsection 42V(6C) |
54 Offences and forfeiture
(3) If a court:
(a) convicts a person of an offence against this Act; or
(aa) makes an order under section 19B of the Crimes Act 1914 in respect of a person charged with an offence against this Act; or
(b) orders a person to pay a pecuniary penalty for the contravention of a civil penalty provision;
in relation to any therapeutic goods, the court may order that the goods be forfeited to the Commonwealth and, if an order is made, the goods become the property of the Commonwealth.
(4) Where goods are so forfeited, the Secretary may cause notice of the forfeiture to be published in the Gazette or on the Department’s website.
(5) Goods forfeited under an order referred to in subsection (3) are to be disposed of in such manner as the Secretary directs.
54AA Offences for contravening conditions or requirements imposed under the regulations
(1) If:
(a) a person holds a licence or a permission to import or export therapeutic goods; and
(b) the person engages in conduct; and
(c) the conduct breaches a condition or a requirement to which the licence or permission is subject under the regulations;
the person commits an offence punishable on conviction by a fine of no more than the number of penalty units specified in whichever of subsection (2) or (3) applies.
(1A) In subsection (1):
engage in conduct means:
(a) do an act; or
(b) omit to perform an act.
(2) If:
(a) the condition or requirement relates to the possession, custody, transport, use or disposal of the goods; or
(b) the regulation providing for the condition or requirement states that the purpose of the condition or requirement is to protect the safety of the public;
the number of penalty units for the contravention is 240 penalty units.
(3) If subsection (2) does not apply, the number of penalty units for the contravention is 50 penalty units.
54AB Criminal offence for damaging etc. documents
(1) A person commits an offence if:
(a) the person damages, destroys, alters, conceals or falsifies a document; and
(b) the document is created, retained or issued for the purposes of this Act, or for purposes that include the purposes of this Act.
Penalty: 7 years imprisonment or 2,000 penalty units, or both.
Note: For the liability of an executive officer of a body corporate, see sections 54B and 54BA.
(2) Strict liability applies to paragraph (1)(b).
Note: For strict liability, see section 6.1 of the Criminal Code.
54AC Civil penalty for damaging etc. documents
A person contravenes this section if:
(a) the person damages, destroys, alters, conceals or falsifies a document; and
(b) the document is created, retained or issued for the purposes of this Act, or for purposes that include the purposes of this Act; and
(c) the damage, destruction, alteration, concealment or falsification is likely to interfere with the proper administration of this Act or the regulations.
Maximum civil penalty:
(a) for an individual—5,000 penalty units; and
(b) for a body corporate—50,000 penalty units.
54A Time for bringing prosecutions
A prosecution for an offence against this Act may be commenced at any time within 3 years after the commission of the offence.
54B Personal liability of an executive officer of a body corporate—general
(1) An executive officer of a body corporate commits an offence if:
(a) the body corporate commits an offence against this Act covered by section 54BA; and
(b) the officer knew that the offence would be committed; and
(c) the officer was in a position to influence the conduct of the body in relation to the commission of the offence; and
(d) the officer failed to take all reasonable steps to prevent the commission of the offence.
Note: An offence against this Act includes an offence against the regulations: see subsection 3(7).
(2) The maximum penalty for an offence against subsection (1) is:
(a) the maximum penalty that a court could impose in respect of an individual for the offence committed by the body corporate; or
(b) if the offence committed by the body corporate is an offence against subsection 41MN(10)—imprisonment for 5 years or 4,000 penalty units, or both.
(3) An executive officer of a body corporate contravenes this subsection if:
(a) the body corporate contravenes a civil penalty provision; and
(b) the officer knew that the contravention would occur; and
(c) the officer was in a position to influence the conduct of the body in relation to the contravention; and
(d) the officer failed to take all reasonable steps to prevent the contravention.
(4) The maximum civil penalty for a contravention of subsection (3) is:
(a) the maximum civil penalty that a court could impose in respect of an individual for the civil penalty provision contravened by the body corporate; or
(b) if the civil penalty provision contravened by the body corporate is subsection 41MNA(3)—5,000 penalty units.
(5) In this section:
executive officer of a body corporate means a person, by whatever name called and whether or not a director of the body, who is concerned in, or takes part in, the management of the body.
54BA Personal liability of an executive officer of a body corporate—offences covered
For the purposes of paragraph 54B(1)(a), this section covers offences against:
(a) the provisions of this Act listed in the following table; and
(b) a provision of a regulation prescribed for the purpose of this paragraph; and
(c) section 6 of the Crimes Act 1914, or section 11.1, 11.4 or 11.5 of the Criminal Code, in relation to an offence mentioned in paragraph (a) or (b) of this subsection; and
(d) section 136.1, 137.1 or 137.2 of the Criminal Code in relation to this Act or a regulation.
Corporate offences for which executive officers may be personally liable |
Item | Provisions of this Act |
1 | Subsection 9G(1) |
2 | Subsection 14(1), (6) or (10) |
3 | Subsection 15(2) |
4 | Subsection 19B(1) |
4A | Subsection 21A(1) or (5) |
5 | Subsection 22(2) or (7AB) |
6 | Subsection 22A(1) |
7 | Subsection 29A(1) |
8 | Subsection 29B(3) or (4) |
9 | Subsection 30EC(1) |
10 | Subsection 30F(4B) |
11 | Subsection 31(5A) |
12 | Subsection 31D(1) |
13 | Subsection 31E(1) |
14 | Subsection 32BA(1) |
15 | Subsection 32BB(1) |
16 | Subsection 32BC(1) |
17 | Subsection 32BD(1) |
17A | Subsection 32BJ(2A) |
18 | Subsection 32CH(1) |
19 | Subsection 32CJ(6) |
20 | Subsection 32DO(1) |
21 | Subsection 32DQ(1) |
22 | Subsection 32DR(3) or (4) |
23 | Subsection 32EF(1) |
24 | Subsection 32HC(1) |
25 | Subsection 32JB(2) |
26 | Subsection 32JI(2) |
27 | Subsection 35(1) or (5) |
27AA | Subsection 35B(1) |
27A | Subsection 41AD(1) |
27B | Subsection 41AE(1) |
28 | Subsection 41EI(1) |
29 | Subsection 41FE(1) |
30 | Subsection 41JB(4) |
31 | Subsection 41JH(1) |
32 | Subsection 41JI(1) |
33 | Subsection 41KC(1) |
34 | Subsection 41MA(1), (5) or (9) |
35 | Subsection 41MC(2) |
36 | Subsection 41ME(1) or (5) |
37 | Subsection 41MF(1) or (3) |
38 | Section 41MH |
39 | Subsection 41MI(1) |
39A | Subsection 41ML(1) |
40 | Subsection 41MN(1), (5) or (10) |
41 | Subsection 41MNB(1) |
42 | Subsection 41MP(1) |
43 | Subsection 41MQ(3) or (4) |
43A | Subsection 42DL(1) |
43B | Subsection 42DLA(1) |
43C | Subsection 42DM(1) |
43D | Subsection 42DW(1) |
44 | Subsection 42E(1) |
45 | Subsection 42T(1) or (2) |
46 | Subsection 42V(6) |
47 | Subsection 42W(1) or (2) |
48 | Subsection 54AB(1) |
54C Establishing whether an executive officer took reasonable steps to prevent the commission of an offence or the contravention of a civil penalty provision
(1) For the purposes of section 54B, in determining whether an executive officer of a body corporate failed to take all reasonable steps to prevent the commission of the offence or the contravention of a civil penalty provision, a court is to have regard to:
(a) what action (if any) the officer took towards ensuring that the body’s employees, agents and contractors have a reasonable knowledge and understanding of the requirements to comply with this Act and the regulations, in so far as those requirements affect the employees, agents or contractors concerned; and
(b) what action (if any) the officer took when he or she became aware that the body was committing an offence against, or otherwise contravening, this Act or the regulations.
(2) This section does not, by implication, limit the generality of section 54B.
(3) In this section, executive officer has the same meaning as in section 54B.
55 Conduct by directors, employees and agents
(1) Where, in proceedings for an offence against this Act, or for a contravention of a civil penalty provision, it is necessary to establish the state of mind of a body corporate in relation to particular conduct, it is sufficient to show:
(a) that the conduct was engaged in by a director, employee or agent of the body corporate within the scope of his or her actual or apparent authority; and
(b) that the director, employee or agent had the state of mind.
(2) Any conduct engaged in on behalf of a body corporate by a director, employee or agent of the body corporate within the scope of his or her actual or apparent authority is to be taken, for the purposes of a prosecution for an offence against this Act, or for a contravention of a civil penalty provision, to have been engaged in also by the body corporate unless the body corporate establishes that the body corporate took reasonable precautions and exercised due diligence to avoid the conduct.
(3) Where, in proceedings for an offence against this Act, or for a contravention of a civil penalty provision, it is necessary to establish the state of mind of a person other than a body corporate in relation to particular conduct, it is sufficient to show that:
(a) the conduct was engaged in by an employee or agent of the person within the scope of his or her actual or apparent authority; and
(b) the employee or agent had the state of mind.
(4) Any conduct engaged in on behalf of a person other than a body corporate (in this subsection called the employer) by an employee or agent of the employer within the scope of his or her actual or apparent authority is to be taken, for the purposes of a prosecution for an offence against this Act, or for a contravention of a civil penalty provision, to have been engaged in also by the employer unless the employer establishes that he or she took reasonable precautions and exercised due diligence to avoid the conduct.
(5) Where:
(a) a person other than a body corporate is convicted of an offence; and
(b) the person would not have been convicted of the offence if subsections (3) and (4) had not been enacted;
the person is not liable to be punished by imprisonment for that offence.
(6) A reference in subsection (1) or (3) to the state of mind of a person includes a reference to:
(a) the knowledge, intention, opinion, belief or purpose of the person; and
(b) the person’s reasons for the intention, opinion, belief or purpose.
(7) A reference in this section to a director of a body corporate includes a reference to a constituent member of a body corporate incorporated for a public purpose by a law of the Commonwealth, of a State or of a Territory.
(8) A reference in this section to engaging in conduct includes a reference to failing or refusing to engage in conduct.
56 Judicial notice
All courts (except in proceedings under Chapter 4) are to take judicial notice of the British Pharmacopoeia, the European Pharmacopoeia, the United States Pharmacopeia‑National Formulary, a homoeopathic pharmacopoeia and an anthroposophic pharmacopoeia.
56A Certificates to provide evidence of certain matters
(1) The Secretary or a person authorised in writing by him or her to give certificates under this section may certify in writing that, at a specified time, or at all times during a specified period:
(a) there was no exemption in effect under section 18 or 18A in relation to particular therapeutic goods; or
(aaaa) a person was not exempt under subsection 32CA(1) in relation to a particular biological or there was no exemption under subsection 32CA(2) in relation to a particular biological; or
(aaab) there was no exemption in effect under section 32CB in relation to a particular biological; or
(aaa) there was no exemption in force under section 41GS in relation to a particular kind of medical device; or
(aa) particular medical devices were not exempt devices;
(b) there was no approval under subsection 19(1) or authority under subsection 19(5) granted to a particular person in relation to particular therapeutic goods; or
(baa) there was no approval under subsection 32CK(1) or authority under subsection 32CM(1) granted to a particular person in relation to a particular biological; or
(ba) there was no approval or authority in effect under section 41HB or subsection 41HC(1) granted to a particular person in relation to particular medical devices;
(bb) there was no approval under subsection 41HD(1), (1A) or (2) granted to a particular person in relation to particular medical devices; or
(c) there was no approval under section 19A granted to a particular person in relation to particular therapeutic goods; or
(ca) there was no approval under subsection 32CO(1), (1A) or (2) granted to a particular person in relation to a particular biological; or
(d) particular therapeutic goods were or were not included in the Register as registered goods; or
(da) particular therapeutic goods were or were not included in the Register as provisionally registered goods; or
(e) particular therapeutic goods were or were not included in the Register as listed goods; or
(eaa) a particular biological was or was not included in the Register; or
(ea) particular medical devices were or were not medical devices of a kind included in the Register; or
(eb) particular medical devices were suspended from the Register; or
(f) particular therapeutic goods were included in the Register subject to conditions including those specified in the certificate; or
(g) the registration, listing or inclusion in the Register of the particular therapeutic goods had been suspended or cancelled; or
(h) there was no declaration under section 7 which applied to particular therapeutic goods; or
(ha) there was no determination under section 7AA which applied to particular goods; or
(i) a person was or was not the holder of a licence in force under Part 3‑3; or
(j) the licence is subject to conditions including those specified in the certificate; or
(k) there was no exemption in effect under subsection 34(1) that applied to particular therapeutic goods or a particular class of therapeutic goods; or
(l) there was no exemption in effect under subsection 34(2) that applied to a particular person in relation to one or more of the following:
(i) the manufacture of particular therapeutic goods;
(ii) a particular step in the manufacture of particular therapeutic goods;
(iii) the manufacture of a particular class of therapeutic goods;
(iv) a particular step in the manufacture of a particular class of therapeutic goods; or
(la) there was no conformity assessment body determination in force in respect of a particular Australian corporation; or
(lb) a conformity assessment body determination was in force in respect of a particular Australian corporation and the determination:
(i) was of general application; or
(ii) was limited to the extent specified in the certificate; or
(m) a conformity assessment certificate has been issued relating to a particular kind of medical device; or
(n) a conformity assessment certificate was subject to conditions including those specified in the certificate under this section; or
(o) a conformity assessment certificate was suspended.
(2) A certificate under subsection (1) may relate to more than one of the matters referred to in paragraphs (1)(a) to (o).
(3) In proceedings for an offence against this Act or a contravention of a civil penalty provision, a certificate under subsection (1) is prima facie evidence of the matters specified in the certificate.
(4) In proceedings for:
(a) an offence against section 14 or 41MA; or
(b) the contravention of section 14A or 41MAA (civil penalty provisions);
a certificate by the Secretary to the effect that:
(c) the Secretary did not consent to the importation, supply or exportation that is the subject of the proceedings; or
(d) the Secretary consented to that importation, supply or exportation subject to conditions specified in the certificate;
is prima facie evidence of the matters specified in the certificate.
(5) In proceedings for an offence against this Act or a contravention of a civil penalty provision, a document purporting to be a certificate given under this section is, unless the contrary is proved, taken to be such a certificate and to have been duly given.
57 Delegation
(1) Subject to subsections (2), (6) and (8) to (11), the Minister or the Secretary may, by signed instrument, delegate to:
(a) an officer of the Department; or
(b) an officer of an authority of the Commonwealth that has functions in relation to therapeutic goods; or
(ba) an APS employee in an Agency (within the meaning of the Public Service Act 1999) that has functions in relation to therapeutic goods; or
(c) a person occupying or acting in an office, or holding an appointment, declared by the regulations to be an office or appointment the occupant or holder of which may be a delegate under this section; or
(d) a person seconded to the Department from:
(i) an authority of a State or a Territory that has functions relating to therapeutic goods, health or law enforcement; or
(ii) a national regulatory authority of a foreign country that has national responsibility relating to therapeutic goods, health or law enforcement; or
(iii) an international organisation that has a function relating to therapeutic goods, health or law enforcement;
all or any of his or her powers and functions under this Act.
(2) The powers of the Secretary under paragraph 19(1)(a), 32CK(1)(d) or 41HB(1)(d) may be delegated under subsection (1) only to a person referred to in paragraph (1)(a) or (c) who is registered, or eligible for registration, in a State or internal Territory, as a medical or dental practitioner or as a pharmacist.
(3) Subject to the regulations, the Secretary may, in such circumstances as are prescribed, by signed instrument, delegate all or any of his or her powers under paragraph 19(1)(a), 32CK(1)(d) or 41HB(1)(d) to a person who is registered, in a State or internal Territory, as a medical or dental practitioner.
(4) A delegate under subsection (3) is, in the exercise of a delegated power, subject to the directions of:
(a) the Secretary; or
(b) an officer of the Department authorised in writing by the Secretary; or
(c) a person referred to in paragraph (1)(c).
(5) Without limiting the generality of matters that may be dealt with by regulations made for the purposes of subsection (3), the regulations may make provision in relation to the following:
(a) the persons who may be delegates;
(b) the circumstances in which delegates may grant approvals for the purposes of paragraph 19(1)(a), 32CK(1)(d) or 41HB(1)(d);
(c) the conditions to which any approvals granted by delegates are to be subject;
(d) requiring information to be given by delegates to the Secretary.
(6) The powers of the Secretary under subsection 19(5), 32CM(1) or 41HC(1) may be delegated only to a person referred to in paragraph (1)(a) or (c) who is registered, or eligible for registration, in a State or internal Territory as a medical or dental practitioner.
(7) The regulations may prescribe the circumstances in which, and the requirements subject to which, delegates may grant authorities under subsection 19(5), 32CM(1) or 41HC(1).
(8) The powers of the Secretary under section 19A or 32CO may be delegated only to a person who holds, occupies or performs the duties of a position in the Department prescribed by the regulations.
(9) The powers of the Secretary under section 41HD may be delegated only to a person who holds, occupies or performs the duties of a position in the Department prescribed by the regulations.
(10) The power of the Minister under subsection 18A(1) may be delegated only to the Secretary.
(10A) The power of the Minister under subsection 32CB(1) may be delegated only to the Secretary.
(11) The power of the Minister under subsection 41GS(1) may be delegated only to the Secretary.
58 Export certifications
(1) The Secretary may issue export certification for goods for therapeutic use in humans, including certifications for the purposes of the World Health Organisation Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce.
(2) A State or Territory must not issue export certifications for goods for therapeutic use in humans.
(3) Such fee as is prescribed is payable in respect of:
(a) an application for a certification under this section; and
(b) where an inspection of a manufacturing site is necessary for the purposes of the issue of a certification under this section—the inspection of that site.
59 Fees
(1) No fees are payable under this Act in respect of an event occurring before 1 July 1990.
(2) Fees prescribed under this Act must not be such as to amount to taxation.
60 Review of decisions
(1) In this section and section 60A:
decision has the same meaning as in the Administrative Appeals Tribunal Act 1975.
initial decision means a decision of the Secretary or of a delegate of the Secretary:
(a) under subsection 7(1) or 41BD(3); or
(aa) under subsection 7C(3); or
(ab) under section 9C, 9D or 9F; or
(b) refusing to grant, or imposing conditions on a grant of, a consent under section 14 or 14A; or
(c) under Part 3‑2 (registration and listing of therapeutic goods), other than a decision under paragraph 26BE(4)(a), or a decision under subsection 26BJ(8), to make a recommendation; or
(ca) under Part 3‑2A (Biologicals); or
(d) under Part 3‑3 (manufacturing of therapeutic goods); or
(e) under Part 4‑4 (conformity assessment certificates); or
(f) under Part 4‑5 (including medical devices in the Register), other than:
(i) a decision under section 41FH (selecting applications for auditing); or
(ii) a decision about which aspects of the matters referred to in paragraphs 41FI(1)(a) and (b) to consider in auditing an application under Subdivision C of Division 1 of Part 4‑5; or
(g) under Part 4‑6 (suspension and cancellation from the Register); or
(h) under Part 4‑7 (exempting medical devices from inclusion in the Register); or
(i) under Part 4‑8 (obtaining information); or
(j) under Part 4‑9 (public notification and recovery of medical devices); or
(k) refusing to grant, or imposing conditions on a grant of, a consent for the purposes of section 41MA or 41MAA (non‑compliance with essential principles); or
(l) under section 42DF, 42DH or 42DI or subsection 42DV(1) or (2).
reviewable decision means a decision of the Minister under subsection (3).
(1A) For the avoidance of doubt, the following are not initial decisions for the purposes of this section or section 60A:
(aaa) the giving of advice under section 22G;
(aa) a preliminary assessment under section 23B, 26BD, 32DDA or 41FDB;
(a) a proposal to suspend a conformity assessment certificate under section 41EM;
(b) a proposal to revoke a conformity assessment certificate under section 41ET;
(c) a proposal to suspend a kind of medical device from the Register under section 41GA;
(d) a proposal to cancel the entry of a kind of medical device on the Register under section 41GN.
(2) Subject to this section, a person whose interests are affected by an initial decision may, by notice in writing given to the Minister:
(a) if this Act requires the person to be given notice in writing of the decision, or of particulars of the decision—within 90 days after the notice is given to the person; or
(b) otherwise—within 90 days after the earlier of:
(i) notice of the decision, or of particulars of the decision, being published in the Gazette or on the Department’s website; and
(ii) the decision first coming to the person’s notice;
request the Minister to reconsider the decision.
(2A) A request under subsection (2) may be accompanied by information in support of the request.
(2AA) If the Secretary or a delegate of the Secretary makes a decision under subsection 9D(1A) or (1B) to vary an entry in the Register in relation to a medicine, a person is not entitled to request the Minister to reconsider the decision unless the person is the person in relation to whom the medicine is registered.
(2AB) If the Secretary or a delegate of the Secretary:
(a) makes a decision under section 22D in relation to an application under section 22C; or
(b) makes a decision under section 22E in relation to an application under subsection 22E(3); or
(d) makes a decision under subsection 25(3) in relation to an application for provisional registration of a medicine;
a person is not entitled to request the Minister to reconsider the decision unless the person made the application.
(2AC) If the Secretary or a delegate of the Secretary makes a decision under section 22F to revoke a provisional determination under section 22D, a person is not entitled to request the Minister to reconsider the decision unless the person made the application for that provisional determination.
(2B) If the Secretary or a delegate of the Secretary decides, under paragraph 26BE(4)(b), to refuse to make a recommendation, a person is not entitled to request the Minister to reconsider the decision unless the person made an application under subsection 26BD(1) for the recommendation.
(2C) If the Secretary or a delegate of the Secretary decides, under subsection 26BJ(8), to refuse to make a recommendation, a person is not entitled to request the Minister to reconsider the decision unless the person made an application under subsection 26BJ(1) for the recommendation.
(2D) If the Secretary or a delegate of the Secretary:
(a) makes a decision under subsection 29(6) or (6A) in relation to an application under subsection 29(4); or
(b) makes a decision under subsection 29(9) to end, or extend, the provisional registration period for a medicine;
a person is not entitled to request the Minister to reconsider the decision unless the person is the person in relation to whom the medicine is provisionally registered.
(3) Subject to paragraph 60A(2)(b), the Minister must, as soon as practicable after receiving a request under subsection (2), reconsider the initial decision and, as a result of that reconsideration, may:
(a) confirm the initial decision; or
(b) revoke the initial decision, or revoke that decision and make a decision in substitution for the initial decision.
(3A) Subject to subsection 60A(2), in reconsidering the initial decision:
(a) the Minister must take into account any information referred to in subsection (2A); and
(b) the Minister must not take into account any other information provided by, or on behalf of, the person after the making of the request, other than:
(i) information provided in response to a request from the Minister; or
(ii) information that indicates that the quality, safety or efficacy of therapeutic goods is unacceptable.
(3B) Paragraph (3A)(a) does not limit the information the Minister may take into account in reconsidering the initial decision.
(3C) If, under paragraph (3)(b), the Minister revokes an initial decision and makes a decision in substitution for the initial decision then the substituted decision:
(a) is taken to be a decision of the Secretary (except for the purpose of any review of the substituted decision); and
(b) has effect, or is taken to have had effect, on and from the date determined by the Minister.
(4) Where a person who has made a request under subsection (2) does not receive notice of the decision of the Minister on reconsideration, or (if applicable) notice that the matter has been remitted under paragraph 60A(2)(b), within 60 days of the making of the request, the Minister is taken to have confirmed under subsection (3) the initial decision.
(5) After reconsideration of an initial decision, the Minister must give the applicant a notice in writing stating the result of the reconsideration and that the applicant may, except where subsection 28(4) of the Administrative Appeals Tribunal Act 1975 applies, apply for a statement setting out the reasons for the decision on reconsideration and may, subject to that Act, make an application to the Administrative Appeals Tribunal for review of that decision.
(5A) If:
(a) the initial decision is one the particulars of which are required to be published in the Gazette or on the Department’s website; and
(b) the Minister revokes the initial decision;
the Secretary must, as soon as practicable after the revocation, cause to be published in the Gazette, or on the Department’s website, a notice setting out particulars of the revocation.
(5B) If:
(a) the initial decision is one the particulars of which are required to be published in the Gazette or on the Department’s website; and
(b) the Minister revokes the initial decision and makes a decision (the substituted decision) in substitution for the initial decision;
the Secretary must, as soon as practicable after the substituted decision is made, cause to be published in the Gazette, or on the Department’s website, a notice setting out particulars of the substituted decision.
(6) Where written notice of the making of an initial decision is given to a person whose interests are affected by the decision, the notice is to include a statement to the effect that a person whose interests are affected by the decision may:
(a) seek a reconsideration of the decision under this section; and
(b) subject to the Administrative Appeals Tribunal Act 1975, if the person is dissatisfied with the decision upon reconsideration, make an application to the Administrative Appeals Tribunal for review of that decision.
(7) Any failure to comply with the requirements of subsection (5) or (6) in relation to a decision does not affect the validity of the decision.
(8) An application may be made to the Administrative Appeals Tribunal for review of a reviewable decision.
60A New information on review—discretion to remit
(1) This section applies only if the Secretary or an authorised delegate makes a decision under section 25, 32DF, 32DG or 41EC in relation to therapeutic goods.
(2) If a person (the appellant) whose interests are affected by the decision requests the Minister to reconsider the decision, and lodges initial new information in support of that request, the Minister must either:
(a) take that information into account when he or she reconsiders the decision; or
(b) remit the matter to an authorised delegate for a fresh decision.
(3) If the appellant applies to the Administrative Appeals Tribunal for review of the decision on reconsideration, and lodges initial new information or later new information (or both) in support of that application, the Tribunal may, if the Tribunal thinks fit, remit the matter to an authorised delegate for a fresh decision.
(4) If:
(a) the appellant applies to the Administrative Appeals Tribunal for review of the decision on reconsideration and lodges initial new information in support of that application; and
(b) the appellant does not lodge later new information in support of that application;
the Tribunal must not remit the matter under subsection (3) if all of the initial new information is information that the Minister took into account under paragraph (2)(a) in making the decision on reconsideration.
(5) If:
(a) the appellant lodges initial new information or later new information (or both) in support of an application to the Administrative Appeals Tribunal for review of the decision on reconsideration; and
(b) the Tribunal does not remit the matter under subsection (3);
the Tribunal, in reviewing the decision on reconsideration:
(c) may consider initial new information (if any) that the Minister took into account under paragraph (2)(a) in making the decision on reconsideration; and
(d) must not consider any other initial new information, except initial new information that indicates that the quality, safety or efficacy of the therapeutic goods is unacceptable; and
(e) must not consider any later new information, except later new information that indicates that the quality, safety or efficacy of the therapeutic goods is unacceptable.
(6) If:
(aa) the matter relates to a decision under section 25; and
(a) the Minister or the Tribunal remits the matter; and
(b) the appellant has paid, as a further evaluation fee, the evaluation fee that the appellant would have to pay under section 24 on making a new application for registration of the therapeutic goods;
the authorised delegate must make a decision under section 25, taking into account the initial new information or later new information (or both), as the case may be, as if a fresh application for registration had been made.
(6AA) If:
(a) the matter relates to a decision under section 32DF or 32DG; and
(b) the Minister or the Tribunal remits the matter; and
(c) the appellant has paid, as a further evaluation fee, the evaluation fee that the appellant would have to pay under section 32DI on making a new application for inclusion of the biological in the Register;
the authorised delegate must make a decision whether or not to include the biological in the Register, taking into account the initial new information or later new information (or both), as the case may be, as if a fresh application for inclusion of the biological in the Register had been made.
(6A) If:
(a) the matter relates to a decision under section 41EC; and
(b) the Minister or the Tribunal remits the matter; and
(c) the appellant has paid, as a further conformity assessment fee, the conformity assessment fee that the appellant would have to pay under section 41LA on making a new application for a conformity assessment certificate;
the authorised delegate must make a decision under section 41EC, taking into account the initial new information or later new information (or both), as the case may be, as if a fresh application for a conformity assessment certificate had been made.
(7) To remove any doubt, the authorised delegate’s fresh decision is to be treated, for the purposes of subsequent applications of section 60 and this section, as a decision under Part 3‑2, 3‑2A or 4‑4.
(8) In this section:
authorised delegate means a delegate of the Secretary:
(a) exercising a power to decide whether to register therapeutic goods; or
(aa) exercising a power to decide whether to include a biological in the Register; or
(b) exercising a power to decide whether to issue a conformity assessment certificate.
initial new information means information that:
(a) was in existence at the time the decision referred to in subsection (1) was made; and
(b) was not made available to the Secretary or authorised delegate for the purpose of making that decision; and
(c) is relevant to that decision;
and includes any opinions that are wholly or substantially based on such information (whether the opinions were formed before or after that decision was made).
later new information means information that:
(a) was in existence at the time the decision on reconsideration was made; and
(b) was not made available to the Minister or delegate of the Minister for the purpose of making that decision; and
(c) is relevant to that decision;
and includes any opinions that are wholly or substantially based on such information (whether the opinions were formed before or after that decision was made).
61 Release of information
(1) In this section:
therapeutic goods information means information in relation to therapeutic goods that is held by the Department and relates to the performance of the Department’s functions (including functions relating to the EC Mutual Recognition Agreement, the EFTA Mutual Recognition Agreement or the Australia‑UK Mutual Recognition Agreement).
(2) The Secretary may:
(a) release to the World Health Organisation therapeutic goods information relating to:
(i) notifications concerning therapeutic goods the consumption or supply of which in Australia has been prohibited or severely restricted, or relating to the reasons for that action; or
(ii) the licensing status of Australian manufacturers of therapeutic goods and their compliance with the manufacturing principles; or
(iii) the content of reports to the Department concerning adverse effects of therapeutic goods; or
(iv) the issue of, imposition of conditions on, or revocation of, conformity assessment certificates;
for use in the development of policies relating to the regulation of therapeutic goods or for the provision of information to regulatory authorities of member countries of the World Health Organisation; or
(b) release, in confidence, therapeutic goods information to the World Health Organisation, being information concerning proceedings of committees established under the regulations.
(3) The Secretary may release to an authority of the Commonwealth, a State or a Territory that has functions relating to therapeutic goods, therapeutic goods information relating to:
(a) reported problems and complaints concerning therapeutic goods, the Department’s investigation of those problems and complaints and any action that the Department has taken or proposes to take in relation to those problems and complaints; or
(b) reports of inspections conducted under this Act or the regulations; or
(c) decisions to revoke or suspend, or not to issue, licences for the manufacturing of therapeutic goods; or
(d) conditions of licences; or
(e) reports of the testing of samples of therapeutic goods; or
(f) the issue of, imposition of conditions on, or revocation of, conformity assessment certificates;
for use in the performance of those functions.
(3A) The Secretary may release information obtained in response to a notice under section 31A, 31AA, 31B, 31BA, 32JE, 32JF, 32JG, 32JH, 41AB, 41JCA, 41JD, 41JE or 41JF to:
(a) an authority of the Commonwealth, a State or a Territory that has functions relating to therapeutic goods; and
(b) the body in a State or Territory responsible for the registration of medical practitioners in that State or Territory; and
(c) the body in a State or Territory responsible for the registration of pharmacists in that State or Territory.
(4) The Secretary may release to a national regulatory authority of another country, being an authority that has national responsibility relating to therapeutic goods, therapeutic goods information relating to:
(a) recommendations of advisory committees on therapeutic goods supplied in or proposed for supply in Australia, and any conditions that are or will be applicable to that supply; or
(b) decisions on the registration or listing, or the suspension or cancellation of the registration or listing, of therapeutic goods; or
(baa) decisions on the inclusion of biologicals in the Register, or the suspension or cancellation of the inclusion of biologicals in the Register; or
(ba) decisions on the inclusion of kinds of medical devices in the Register, or the suspension or cancellation of the inclusion of kinds of medical devices in the Register; or
(c) the withdrawal from supply in Australia of therapeutic goods and the reasons for that action; or
(d) the licensing status of Australian manufacturers of therapeutic goods and their compliance with the manufacturing principles; or
(e) proceedings of committees established under the regulations; or
(f) the issue of, imposition of conditions on, or revocation of, conformity assessment certificates;
for use in the performance of those functions or for furthering international co‑operation in the regulation of therapeutic goods.
(4A) The Secretary may release to:
(a) an authority of the Commonwealth, a State or a Territory that has functions relating to therapeutic goods, health or law enforcement; or
(b) a national regulatory authority of another country that has national responsibility relating to therapeutic goods, health or law enforcement; or
(ba) an international organisation that has a function relating to therapeutic goods, health or law enforcement;
therapeutic goods information relating to one or more of the following:
(c) notifications received under section 42T;
(d) action taken by the Secretary under Part 5‑3;
(da) action taken by the Secretary under section 30EA (about notification and recall of therapeutic goods);
(db) action taken by the Secretary under section 32HA (about notification and recall of biologicals);
(dc) action taken by the Secretary under section 41KA (about notification and recall of medical devices);
(e) contraventions, or possible contraventions, of Part 5‑2 or Part 5‑3;
(f) any cases, or possible cases, of actual or potential tampering with therapeutic goods;
(fa) any cases, or possible cases, of counterfeit therapeutic goods;
(g) information relating to an offence committed against this Act, or alleged to have been committed against this Act, involving therapeutic goods;
(h) information relating to the contravention of a civil penalty provision, or the alleged contravention of a civil penalty provision, involving therapeutic goods;
(i) a breach of a requirement of this Act or the regulations.
(4B) The release of therapeutic goods information mentioned in paragraphs (4A)(g), (h) and (i) is not taken, for the purposes of paragraph 6.2(b) of Australian Privacy Principle 6, to be authorised by this Act.
(5) The Secretary may release to a national regulatory authority of another country, or an international organisation, being another country or an organisation with which the Commonwealth has cooperative arrangements relating to the assessment or regulation of therapeutic goods, the following information the release of which is consistent with those arrangements:
(a) therapeutic goods information;
(b) information relating to Australian conformity assessment bodies and either to conformity assessment body determinations or to certification‑related activities of Australian conformity assessment bodies.
(5AA) The Secretary may release to a person, body or authority that is specified, or is of a kind specified, under subsection (5AB) therapeutic goods information of a kind specified under that subsection for a purpose specified under that subsection.
(5AB) For the purpose of subsection (5AA), the Minister may, by legislative instrument, specify one or more of the following:
(a) a person, body or authority;
(b) kinds of persons, bodies or authorities;
(c) kinds of therapeutic goods information;
(d) purposes.
(5A) The Secretary may release to the public therapeutic goods information relating to any decision or action taken under this Act or the regulations.
(5B) The release of therapeutic goods information under subsection (5A) is not taken, for the purposes of paragraph 6.2(b) of Australian Privacy Principle 6, to be authorised by this Act.
(5C) The Secretary may release to the public therapeutic goods information of a kind specified under subsection (5D).
(5D) The Minister may, by legislative instrument, specify kinds of therapeutic goods information for the purpose of subsection (5C).
(6) The Secretary may release to a person, on application by that person, therapeutic goods information of a kind identified in the regulations relating to:
(a) therapeutic goods included in the Register; or
(b) therapeutic goods in relation to which an application for registration, listing or inclusion in the Register has been made.
(6A) Regulations made for the purposes of subsection (6) may:
(a) relate to therapeutic goods generally or to a class of such goods; and
(b) authorise the release of therapeutic goods information to persons generally or to a class of persons.
(7) The Secretary may release therapeutic goods information:
(a) the release of which is necessary to ensure the safe use of particular therapeutic goods; or
(b) relating to the reasons for the withdrawal of therapeutic goods from supply in Australia.
(8) Subject to sections 25A and 26AF, therapeutic goods information provided to the Department in relation to a matter may:
(a) be used by the Department in the consideration of another matter within its functions relating to therapeutic goods; and
(b) be provided to a committee appointed to advise the Minister or the Secretary on matters relating to therapeutic goods, including a committee of the National Health and Medical Research Council.
Note: The Secretary may also disclose therapeutic goods information provided to the Department to the Chief Executive Medicare for the purpose of certain data‑matching: see section 132C of the National Health Act 1953.
(8A) Regulations prescribing fees in respect of applications for information under the regulations:
(a) may include provision for the payment of deposits on account of such fees; and
(b) may provide for fees that take into account the time spent by officers of the Department in:
(i) searching for or retrieving information; or
(ii) making, or doing anything related to the making of, a decision on an application; and
(c) may provide for fees that take into account the direct costs incurred by the Commonwealth in making available an officer to supervise the inspection by an applicant of any document containing information to which an application relates.
(8C) If, under the regulations, a person is liable to pay a fee in respect of an application for information, the Secretary must notify the person, in writing, accordingly, and must give to the person, together with that notification, a statement setting out the basis on which the amount of that fee is calculated.
(10) Nothing in this or any other Act requires the Secretary to disclose to any person, court or tribunal information referred to in subsection 25(2E) (including as that subsection applies because of subsection 32DE(2) or 32EB(3)) or 26(2D) if the disclosure would constitute a breach of the Mutual Recognition Convention.
(11) This section (except subsection (10)) has effect subject to the Freedom of Information Act 1982.
(12) The subsections of this section permitting the release of information have effect independently of each other.
61A Immunity from civil actions
(1) No civil action, suit or proceeding lies against:
(a) the Commonwealth; or
(b) a protected person;
in respect of loss, damage or injury of any kind suffered by another person as a result of anything done, or omitted to be done, by a protected person in relation to the performance or purported performance, or in relation to the exercise or purported exercise, of a protected person’s functions, duties or powers under this Act or the regulations.
(2) Subsection (1) does not apply to an act or omission in bad faith.
(3) A reference in subsection (1) to anything omitted to be done includes a reference to a failure to make a decision.
(4) In this section:
protected person means any of the following:
(a) the Minister;
(b) the Secretary;
(c) a person to whom powers or functions are delegated under subsection 57(1);
(d) a member of a committee established under this Act or the regulations;
(e) an authorised person in relation to a provision of this Act (other than this section);
(f) an authorised officer (within the meaning of the regulations);
(g) an authorised person (within the meaning of the regulations);
(h) a person assisting a person (a primary person) referred to in paragraph (a), (b), (c), (d), (e), (f) or (g) in relation to the performance or purported performance, or in relation to the exercise or purported exercise, of a primary person’s functions, duties or powers under this Act or the regulations.
63 Regulations
(1) The Governor‑General may make regulations, not inconsistent with this Act, prescribing matters:
(a) required or permitted to be prescribed by this Act; or
(b) necessary or convenient to be prescribed for carrying out or giving effect to this Act.
(2) The regulations may:
(a) make provision in relation to:
(i) the establishment of committees to advise the Minister or the Secretary on matters relating to therapeutic goods; and
(ii) the functions and powers of those committees; and
(iii) the payment of remuneration and allowances to members of those committees; and
(b) prescribe requirements for the storage and transport of therapeutic goods; and
(c) prescribe requirements for the advertising of therapeutic goods; and
(d) provide for the procedures to be followed by the Department in the sampling and testing of therapeutic goods; and
(da) provide for the periods within which evaluations under section 25 in relation to specified therapeutic goods or specified classes of such goods are to be completed; and
(daaaa) provide for the periods within which evaluations under section 26AE in relation to specified medicines or specified classes of medicines are to be completed; and
(daaa) provide for the periods within which evaluations under section 26BE in relation to recommendations to vary a section 26BB determination are to be completed; and
(daa) provide for the periods within which evaluations under section 32DE in relation to specified biologicals or specified classes of biologicals are to be completed; and
(db) provide for the periods within which decisions under section 41EP to revoke suspensions of conformity assessment certificates are to be made, in cases where applications for revocation have been made under paragraph 41EP(2)(a); and
(dc) provide for the periods within which decisions on applications for the issuing of conformity assessment certificates under Part 4‑4 are to be made if considering the applications involves examining the design of medical devices; and
(dd) provide for the periods within which decisions under section 41GD to revoke suspensions of entries on the Register are to be made, in cases where applications for revocation have been made under paragraph 41GD(2)(a); and
(de) provide for the periods within which the performance of specified functions conferred on the Secretary by this Act is to be completed; and
(df) provide for the periods within which specified decisions under this Act are to be made by the Secretary; and
(e) prescribe requirements for informational material that is included with therapeutic goods; and
(f) make provision for the transfer of registration, listing or inclusion in the Register of therapeutic goods and of licences; and
(g) make provision for the testing of therapeutic goods, the inspection of manufacturing operations or the evaluation of data concerning therapeutic goods by the Department at the request of persons; and
(h) prescribe fees in respect of matters under this Act or the regulations; and
(j) prescribe penalties not exceeding 10 penalty units for offences against the regulations.
(3) The regulations may:
(a) prescribe different fees under this Act in relation to:
(i) different classes of goods; or
(ii) in the case of fees under Part 3‑3—different steps in the manufacture of goods; or
(b) provide for the refund, reduction or waiving of fees or charges in cases identified in the regulations; or
(c) specify the type of information relating to therapeutic goods manufactured by licence holders that the Secretary may, under subsection 37(2), require to be supplied by the holders of licences at the time of payment of annual licensing charges in respect of the licences.
(3A) The regulations may provide for:
(a) the granting of a licence or permission to import or export therapeutic goods; and
(b) licences or permissions to import or export therapeutic goods to be subject to conditions or requirements; and
(c) the assignment of a licence or permission to import or export therapeutic goods; and
(d) the surrender of a licence or permission to import or export therapeutic goods; and
(e) the revocation of a licence or permission to import or export therapeutic goods.
(4) The regulations may make provision for a matter by applying, adopting or incorporating, with or without modification, any matter contained in an instrument:
(a) as that instrument is in force at the time when the regulations take effect; or
(b) as that instrument is in force from time to time.
(5) For the purposes of section 2, regulations may be made before the commencement of this Act as if this Act were in force, but do not come into effect on a day earlier than the day on which this Act commences.
Chapter 8—Repeal and transitional provisions
66 Transitional arrangements for goods required to be registered or listed
(1) This section applies to therapeutic goods in relation to a person if, immediately before the commencement of this Act, the person was supplying goods of that kind in Australia for use in humans.
(2) Where:
(a) this section applies to therapeutic goods in relation to a person; and
(b) the Secretary is not aware of the person having been convicted of an offence against a law of the Commonwealth, of a State or of an internal Territory in respect of goods of that kind during the period of 2 years ending on the commencement of this Act; and
(c) if the goods are imported goods—the Secretary is not aware of the person having, during that period, imported goods of that kind into Australia otherwise than in accordance with regulations in force under the Customs Act 1901;
subsections 20(1) and (2) do not apply to goods of that kind in relation to the person during the period of 3 months after that commencement.
(3) Where:
(a) this section applies to therapeutic goods in relation to a person; and
(b) the person makes an application for registration or listing of goods of that kind in accordance with section 23 and within 3 months after the commencement of this Act;
then:
(c) subsection 20(1) does not apply to goods of that kind in relation to the person during the period of 6 months after that commencement or before the end of such longer period as the Secretary specifies by notice published in the Gazette before the end of that first‑mentioned period; and
(d) subsection 20(2) does not apply to goods of that kind in relation to the person during the period of 12 months after that commencement or before the end of such longer period as the Secretary specifies by notice published in the Gazette before the end of that first‑mentioned period.
(3A) If, on an application under subsection (3), goods have been registered without having been evaluated, the Secretary may, if he or she thinks it appropriate, give the person in relation to whom the goods are registered written notice that the goods are to be evaluated to determine whether they should continue to be registered.
(4) A person who makes an application in accordance with subsection (3) is not required to pay:
(a) any application fee for the registration or listing of the goods to which the application relates; or
(b) in the case of an application for the registration of goods—any fee for the evaluation of the goods for registration;
but where the goods are later evaluated to determine whether the goods should continue to be registered, such fee as is prescribed is payable in respect of that evaluation.
(4A) In relation to an evaluation conducted for the purposes of this section:
(a) section 25 has effect as if:
(i) the person in respect of whom the goods are registered were an applicant for the registration of the goods; and
(ii) the reference in paragraph (1)(b) to an evaluation fee under section 24 were a reference to a fee payable under subsection (4) of this section; and
(b) sections 24A, 24B and 24C have effect as if any reference in those sections to section 24 were a reference to subsection (4) of this section; and
(c) sections 24D and 24E do not apply.
(4B) If, on an application under subsection (3), goods have been listed without consideration of the matters mentioned in paragraphs 26(1)(c) to (m), the Secretary may, if he or she thinks it appropriate, give the person in relation to whom the goods are listed written notice that the Secretary intends to determine whether the goods should continue to be listed.
(4C) If notice is given under subsection (4B), section 26 applies as if the person in relation to whom the goods are listed were an applicant for the listing of the goods.
(5) Section 21 does not apply, during the period of 15 months after the commencement of this Act or during such longer period as the Secretary specifies by notice published in the Gazette before the end of that first‑mentioned period, to any goods.
(6) Where a person suffers any kind of loss, damage or injury caused by, or arising out of, the use by the person of therapeutic goods to which this section applies, no liability in respect of that loss, damage or injury attaches to the Commonwealth, the Secretary or any delegate of the Secretary.
67 Transitional provision for therapeutic goods for export only
Section 20 does not apply, during the period of 6 months after the commencement of this Act, to therapeutic goods manufactured in Australia solely for export from Australia.
68 Transitional arrangements for Part 3‑3
(1) This section applies to a step in the manufacture of therapeutic goods in relation to a person in relation to premises in Australia if, before the commencement of this Act, the person was carrying out that step in relation to goods of that kind at those premises.
(2) Where:
(a) this section applies to a step in the manufacture of therapeutic goods in relation to a person in relation to premises; and
(b) the Secretary is not aware of the person having been convicted of an offence against a law of the Commonwealth, of a State or of an internal Territory in respect of goods of that kind during the period of 2 years ending on the commencement of this Act;
subsection 35(1) does not apply the carrying out of that step by the person in relation to goods of that kind at those premises during the period of 4 months after that commencement.
(3) Where:
(a) this section applies to a step in the manufacture of therapeutic goods in relation to a person in relation to premises; and
(b) the person makes an application for a licence to carry out that step in relation to goods of that kind at those premises in accordance with section 37 and within 4 months after the commencement of this Act;
subsection 35(1) does not apply to the carrying out of that step by the person in relation to goods of that kind at those premises until the application is determined.
69 Continuation of standards and requirements
Any standards that were in force immediately before the commencement of this Act under Part 2 of the Therapeutic Goods Act 1966, and any requirements that were in force at that time under section 15 of the Therapeutic Goods Act 1966, continue in force as if they were standards made under Part 3‑1 of this Act.
