Federal Register of Legislation
Therapeutic Goods (Standard for Human Albumin) (TGO 111) Order 2022
I, Nick Henderson, as delegate of the Minister for Health and Aged Care, make the following order.
Dated 25 March 2022
Nick Henderson First Assistant Secretary Medicines Regulation Division Health Products Regulation Group Department of Health
Contents 1 Name 2 Commencement 3 Authority 4 Definitions 5 Standard 6 Application 7 Requirements 8 Repeals Schedule 1—Repeals Therapeutic Goods Order No. 90 Standard for human albumin
1 Name (1) This instrument is the Therapeutic Goods (Standard for Human Albumin) (TGO 111) Order 2022. (2) This instrument may also be cited as TGO 111.
2 Commencement (1) Each provision of this instrument specified in column 1 of the table commences, or is taken to have commenced, in accordance with column 2 of the table. Any other statement in column 2 has effect according to its terms.
Commencement information Column 1 Column 2 Column 3 Provisions Commencement Date/Details 1. The whole of this instrument 31 March 2022. 31 March 2022
Note: This table relates only to the provisions of this instrument as originally made. It will not be amended to deal with any later amendments of this instrument. (2) Any information in column 3 of the table is not part of this instrument. Information may be inserted in this column, or information in it may be edited, in any published version of this instrument.
3 Authority This instrument is made under section 10 of the Therapeutic Goods Act 1989.
4 Definitions Note: A number of expressions used in this instrument are defined in subsection 3(1) of the Act, including the following: (a) British Pharmacopoeia; (b) European Pharmacopoeia; (c) export only medicine; (d) standard; (e) therapeutic goods; (f) therapeutic use. In this instrument: Act means the Therapeutic Goods Act 1989. human albumin means albumin derived from humans for: (a) therapeutic use; or (b) use as an ingredient or component in the manufacture of therapeutic goods other than a medical device.
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