Therapeutic Goods (Reportable Medicines) Determination 2025
1Therapeutic Goods (Reportable Medicines) Determination 2025
Start here
Get a plain-English read of 1
Turn the raw legal text into a practical explanation grounded in Therapeutic Goods (Reportable Medicines) Determination 2025.
meta-content-style-type: text/css meta-content-type: application/xhtml+xml; charset=utf-8
?xml version="1.0" encoding="utf-8" standalone="no"?>
Commonwealth Coat of Arms of Australia
Therapeutic Goods (Reportable Medicines) Determination 2025
I, Nicholas Henderson, as delegate of the Minister for Health and Aged Care, make the following determination.
Dated 5 March 2025
Nicholas Henderson
First Assistant Secretary Medicines Regulation Division Health Products Regulation Group Department of Health and Aged Care
Contents
1 Name
2 Commencement
3 Authority
4 Definitions
5 Reportable medicines
6 Repeals
Schedule 1—Reportable Medicines
Schedule 2—Repeals
Therapeutic Goods (Reportable Medicines) Determination 2018
1 Name
This instrument is the Therapeutic Goods (Reportable Medicines) Determination 2025.
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
-
- The whole of this instrument The day after this instrument is registered.
Note: This table relates only to the provisions of this instrument as originally made.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 subsection 30EH(2) 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) active ingredient;
(b) current Poisons Standard;
(c) medicine;