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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.
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- Remove Advertising filter Advertising (2)
- Australian Register of Therapeutic Goods (ARTG) (1) Apply Australian Register of Therapeutic Goods (ARTG) filter
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- Complementary medicines (7) Apply Complementary medicines filter
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- OTC medicines (12) Apply OTC medicines filter
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- (-) Remove Listed medicines filter Listed medicines
- (-) Remove Safety of medicines & medical devices filter Safety of medicines & medical devices
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- (-) Remove Labelling/Packaging filter Labelling/Packaging
- (-) Remove Medical devices safety filter Medical devices safety
- (-) Remove Manufacturing filter Manufacturing
Proposed changes to the Permissible Ingredients Determination: Low-negligible risk changes 2021-22
Closed on 15 September 2021
Proposed improvements to the Therapeutic Goods Advertising Code
Closed on 18 June 2021
IMDRF consultation: Proposed update to document on Post-Market Clinical Follow-Up Studies
Closed on 11 December 2020
Changes to permissible ingredients - Low-negligible risk
Closed on 11 October 2019
The Scheduling Policy Framework and Advertising of Pharmacist-only medicines (Schedule 3 substances)
Closed on 28 April 2017
Labelling project 99/00 Effective by design
Closed on 23 June 2000