Therapeutic Goods Act 1989
THERAPEUTIC GOODS ORDER No. 70C
Standards for Export Only Medicine
I, Larry Kelly, delegate of the Minister for Health for the purposes of section 10 of the Therapeutic Goods Act 1989 (the Act) and acting under that section, having consulted with the Therapeutic Goods Committee in accordance with subsection 10(4) of the Act, HEREBY:
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British Pharmacopoeia, United States Pharmacopoeia and European Pharmacopoeia (as each are defined in subsection 3(1) of the Act) | i) if the medicine is regulated other than as a medicine in the country to which it is to be exported, it meets the regulatory requirements of that country for such products.
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Japanese Pharmacopoeia (16th edition including English language translation of Supplement 1 of April 2013 and partial revision of Supplement 1 of May 2013) | i) the exporter is to hold evidence that a relevant authority of the country to which the medicine is to be exported has confirmed its willingness to accept medicine which complies with this Order, or confirmed that it would have no objection to accepting such medicine, except where the country to which the medicine is to be exported is a country where the medicine is regulated other than as a medicine; and ii) if the medicine is regulated other than as a medicine in the country to which it is to be exported, it meets the regulatory requirements of that country for such products.
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This Order commences on the day after the day it is registered on the Federal Register of Legislative Instruments.
Dated this 16th day of May 2014
(Signed by)
Dr Larry Kelly
Delegate of the Minister for Health