All legislative instruments that are registered must be presented for scrutiny in each House of the Parliament and, unless an exemption applies, they may be disallowed by either House. When documents are presented to the Australian Parliament for scrutiny, they are said to have been tabled.
For transitional provisions relating to the repeal of this standard, see subsections 4(2) and (3) of the Therapeutic Goods (Poisons Standard—February 2023) Instrument 2022.