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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.
Trove at the National Library of Australia has information on archived TGA consultations and reviews.
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- Advertising (2) Apply Advertising filter
- Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG) (1)
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- Complementary medicines (7) Apply Complementary medicines filter
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- Medical devices/IVDs (55) Apply Medical devices/IVDs filter
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- Medicinal cannabis (1) Apply Medicinal cannabis filter
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- OTC medicines (12) Apply OTC medicines filter
- Remove Other therapeutic goods filter Other therapeutic goods (1)
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- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
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- (-) Remove Labelling/Packaging filter Labelling/Packaging
- (-) Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG)
- (-) Remove Medical devices safety filter Medical devices safety
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- (-) Remove Manufacturing filter Manufacturing
- (-) Remove Other therapeutic goods filter Other therapeutic goods
- (-) Remove Biologicals filter Biologicals
Priority Review pathway for biologicals: feasibility, potential eligibility criteria and determination process
Closed on 28 March 2022
Consultation on potential regulatory options for 'export only' biologicals
Closed on 20 December 2021
Remaking of standards and legislative instruments for human cell and tissue (HCT) products, blood and blood components
Closed on 11 July 2021
Proposed improvements to the Therapeutic Goods Advertising Code
Closed on 18 June 2021
Standard for vaporiser nicotine (TGO 110)
Closed on 31 March 2021
Proposal for clarifying regulatory requirements for residual claims for disinfectants
Closed on 26 March 2021
Potential reforms to medicinal cannabis manufacturing, labelling and packaging requirement
Closed on 29 January 2021
IMDRF consultation: Proposed update to document on Post-Market Clinical Follow-Up Studies
Closed on 11 December 2020
Public access to information contained in ARTG entries for therapeutic goods
Closed on 3 February 2006
Labelling project 99/00 Effective by design
Closed on 23 June 2000