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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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- Advertising (8) Apply Advertising filter
- Australian Register of Therapeutic Goods (ARTG) (1) Apply Australian Register of Therapeutic Goods (ARTG) filter
- Biologicals (9) Apply Biologicals filter
- Blood and blood components (4) Apply Blood and blood components filter
- Remove Complementary medicines filter Complementary medicines (22)
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- Labelling/Packaging (23) Apply Labelling/Packaging filter
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- Medical devices safety (1) Apply Medical devices safety filter
- Medical devices/IVDs (48) Apply Medical devices/IVDs filter
- Medicinal cannabis (1) Apply Medicinal cannabis filter
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- OTC medicines (31) Apply OTC medicines filter
- Prescription medicines (25) Apply Prescription medicines filter
- Safety of medicines & medical devices (2) Apply Safety of medicines & medical devices filter
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- Therapeutic Goods Administration (TGA) (6) Apply Therapeutic Goods Administration (TGA) filter
- Therapeutic goods regulation (6) Apply Therapeutic goods regulation filter
Permissible ingredients annual changes 2020-21
Closed on 6 October 2020
Changes to permissible ingredients - Low-negligible risk
Closed on 11 October 2019
Options for the implementation of a claimer for efficacy assessed non-prescription medicines
Closed on 21 June 2018
Discontinuing pre-market evaluation of Herbal Component Names (HCNs)
Closed on 12 January 2018
Business process improvements supporting complementary medicines assessment pathways
Closed on 7 November 2017
Reforms to the regulatory framework for complementary medicines: Assessment pathways
Closed on 28 March 2017
TGA adoption of two European Union (EU) scientific guidelines for herbal medicines
Closed on 10 April 2015
ARGCM Part D: Registered complementary medicines
Closed on 22 July 2013
International harmonisation of ingredient names
Closed on 10 July 2013