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 arrangements relating to the repeal of this instrument, see section 7 of the Therapeutic Goods (Standards for Biologicals—General and Specific Requirements) (TGO 109) Order 2021.