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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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- Remove Advertising filter Advertising (2)
- Australian Register of Therapeutic Goods (ARTG) (1) Apply Australian Register of Therapeutic Goods (ARTG) filter
- Biologicals (2) Apply Biologicals filter
- Remove Blood and blood components filter Blood and blood components (0)
- Complementary medicines (7) Apply Complementary medicines filter
- Fees/Payments (1) Apply Fees/Payments filter
- Remove Import/Export filter Import/Export (1)
- Labelling/Packaging (1) Apply Labelling/Packaging filter
- Legislation (3) Apply Legislation filter
- Listed medicines (2) Apply Listed medicines filter
- Manufacturing (1) Apply Manufacturing filter
- Remove Medical devices/IVDs filter Medical devices/IVDs (55)
- Medical devices safety (1) Apply Medical devices safety filter
- Medicinal cannabis (1) Apply Medicinal cannabis filter
- Remove Medicines filter Medicines (2)
- Medicines safety (1) Apply Medicines safety filter
- OTC medicines (12) Apply OTC medicines filter
- Other therapeutic goods (1) Apply Other therapeutic goods filter
- Remove Prescription medicines filter Prescription medicines (7)
- Scheduling (56) Apply Scheduling filter
- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
- Remove Therapeutic goods regulation filter Therapeutic goods regulation (3)
- (-) Remove Import/Export filter Import/Export
- (-) Remove Blood and blood components filter Blood and blood components
- (-) Remove Therapeutic goods regulation filter Therapeutic goods regulation
- (-) Remove Advertising filter Advertising
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
- (-) Remove Medicines filter Medicines
- (-) Remove Prescription medicines filter Prescription medicines
Consultations on adoption of European Union guidelines in Australia
Closed on 7 February 2020
Export of therapeutic goods from Australia
Closed on 3 February 2020
Review of the regulation of certain self-testing IVDs in Australia
Closed on 6 December 2019
Proposed clarification of the regulatory requirements for medical device systems and procedure packs
Closed on 31 October 2019
Products used for and by people with disabilities
Closed on 25 October 2019
Proposed changes to medical device essential principles for safety and performance
Closed on 17 October 2019
IMDRF consultation: Good Regulatory Review Practices - Requirements for Conformity Assessment Bodies
Closed on 3 October 2019
Proposed clarification that goods are therapeutic goods - goods containing folate substances in certain circumstances
Closed on 18 September 2019
IMDRF consultation: Personalised Medical Devices - Regulatory Pathways
Closed on 24 July 2019