
You are here
Consultations
We conduct public consultations as part of our broader stakeholder engagement work, including on changes to regulatory requirements or practices, reviews of business processes, standards or guidelines, and TGA fees and charges.
Trove at the National Library of Australia has information on archived TGA consultations and reviews.
Filters
Status
Categories
- Remove Advertising filter Advertising (2)
- Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG) (1)
- Biologicals (2) Apply Biologicals filter
- Complementary medicines (7) Apply Complementary medicines filter
- Fees/Payments (1) Apply Fees/Payments filter
- Import/Export (1) Apply Import/Export filter
- Remove Labelling/Packaging filter Labelling/Packaging (1)
- Legislation (3) Apply Legislation filter
- Remove Listed medicines filter Listed medicines (2)
- Manufacturing (1) Apply Manufacturing filter
- Remove Medical devices/IVDs filter Medical devices/IVDs (55)
- Medical devices safety (1) Apply Medical devices safety filter
- Remove Medicinal cannabis filter Medicinal cannabis (1)
- Medicines (2) Apply Medicines filter
- Medicines safety (1) Apply Medicines safety filter
- Remove OTC medicines filter OTC medicines (12)
- Other therapeutic goods (1) Apply Other therapeutic goods filter
- Prescription medicines (7) Apply Prescription medicines filter
- Remove Scheduling filter Scheduling (56)
- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
- Therapeutic goods regulation (3) Apply Therapeutic goods regulation filter
- (-) Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG)
- (-) Remove Listed medicines filter Listed medicines
- (-) Remove Scheduling filter Scheduling
- (-) Remove Medicinal cannabis filter Medicinal cannabis
- (-) Remove OTC medicines filter OTC medicines
- (-) Remove Labelling/Packaging filter Labelling/Packaging
- (-) Remove Advertising filter Advertising
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
Proposed amendments to the Poisons Standard - ACCS, ACMS and joint ACCS/ACMS meetings, June 2022
Closed on 27 May 2022
Notice of interim decisions on proposed amendments to the Poisons Standard – ACMS #36 ACCS #32 Joint ACMS-ACCS #29 - November 2021
Closed on 11 April 2022
Notice of interim decisions on proposed amendments to the Poisons Standard – Joint ACMS-ACCS #25 - June 2020
Closed on 11 April 2022
Proposed amendments to the Poisons Standard - ACCS, ACMS and joint ACCS/ACMS meetings, March 2022
Closed on 31 January 2022
Discussion paper on potential for mandatory reporting of medical device adverse events by healthcare facilities in Australia
Closed on 13 December 2021
Notice of interim decisions on proposed amendments to the Poisons Standard (sodium nitrite) - June 2021
Closed on 11 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard – ACCS #31 – June 2021
Closed on 11 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard - Joint ACMS-ACCS #28 - June 2021
Closed on 11 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard - ACMS #34 - June 2021
Closed on 1 November 2021