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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
- Remove Biologicals filter Biologicals (9)
- Blood and blood components (4) Apply Blood and blood components filter
- Remove Complementary medicines filter Complementary medicines (22)
- Cosmetics (2) Apply Cosmetics filter
- Disinfectants/Sterilants (4) Apply Disinfectants/Sterilants filter
- Import/Export (1) Apply Import/Export filter
- Labelling/Packaging (23) Apply Labelling/Packaging filter
- Legislation (20) Apply Legislation filter
- Listed medicines (2) Apply Listed medicines filter
- Manufacturing (11) Apply Manufacturing filter
- 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
- Medicines (1) Apply Medicines filter
- 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
- Scheduling (37) Apply Scheduling filter
- 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
Draft standards for faecal microbiota transplant (FMT) products
Closed on 31 January 2020
Options for the regulation of Faecal Microbiota Transplantation materials
Closed on 15 March 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
Nomenclature of Biological Medicines
Closed on 8 September 2017
Reforms to the regulatory framework for complementary medicines: Assessment pathways
Closed on 28 March 2017
Consultation on adoption of a European Union guideline in Australia
Closed on 16 December 2016
Guidance on biovigilance responsibilities of sponsors of biologicals
Closed on 16 December 2016