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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
- Remove Biologicals filter Biologicals (2)
- Complementary medicines (7) Apply Complementary medicines filter
- Remove Disinfectants/Sterilants filter Disinfectants/Sterilants (0)
- Fees/Payments (1) Apply Fees/Payments filter
- Import/Export (1) Apply Import/Export filter
- Labelling/Packaging (1) Apply Labelling/Packaging filter
- Legislation (3) Apply Legislation filter
- Remove Listed medicines filter Listed medicines (2)
- Remove Manufacturing filter Manufacturing (1)
- 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
- Prescription medicines (7) Apply Prescription medicines filter
- Scheduling (56) Apply Scheduling filter
- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
- Therapeutic goods regulation (3) Apply Therapeutic goods regulation filter
- (-) Remove Listed medicines filter Listed medicines
- (-) Remove Manufacturing filter Manufacturing
- (-) Remove Advertising filter Advertising
- (-) Remove Biologicals filter Biologicals
- (-) Remove Disinfectants/Sterilants filter Disinfectants/Sterilants
- (-) Remove Medicines filter Medicines
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
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
Changes to permissible ingredients - Low-negligible risk
Closed on 11 October 2019
IMDRF consultation: Good Regulatory Review Practices - Requirements for Conformity Assessment Bodies
Closed on 3 October 2019
IMDRF consultation: Personalised Medical Devices - Regulatory Pathways
Closed on 24 July 2019
Proposed new classification rule for medical devices that administer medicines or biologicals by inhalation
Closed on 29 April 2019