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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
- Australian Register of Therapeutic Goods (ARTG) (1) Apply Australian Register of Therapeutic Goods (ARTG) filter
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- Complementary medicines (7) Apply Complementary medicines filter
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- 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
- Medicines (2) Apply Medicines filter
- Medicines safety (1) Apply Medicines safety filter
- Remove OTC medicines filter OTC medicines (12)
- Other therapeutic goods (1) Apply Other therapeutic goods filter
- Prescription medicines (7) Apply Prescription medicines filter
- Remove Safety of medicines & medical devices filter Safety of medicines & medical devices (0)
- Scheduling (56) Apply Scheduling filter
- Remove Therapeutic Goods Administration (TGA) filter Therapeutic Goods Administration (TGA) (2)
- Therapeutic goods regulation (3) Apply Therapeutic goods regulation filter
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
- (-) Remove Safety of medicines & medical devices filter Safety of medicines & medical devices
- (-) Remove Therapeutic Goods Administration (TGA) filter Therapeutic Goods Administration (TGA)
- (-) Remove OTC medicines filter OTC medicines
Medical device cyber security
Closed on 14 February 2019
Proposal for the regulation of IVD companion diagnostics
Closed on 14 December 2018
IMDRF consultation: Terminologies for categorised adverse event reporting
Closed on 12 October 2018
IMDRF consultation: Unique Device Identification system
Closed on 12 October 2018
IMDRF consultation: Principles of labelling for medical devices and IVD medical devices
Closed on 12 September 2018
Proposed regulatory changes related to personalised and 3D printed medical devices
Closed on 22 December 2017
Alignment with European medical device regulatory framework
Closed on 25 August 2017
Comparable overseas regulators - medical devices
Closed on 30 June 2017
Designation of Australian conformity assessment bodies for medical devices - Implementation
Closed on 11 January 2017
Accelerated assessment of medical devices - Priority Review pathway - Implementation
Closed on 11 January 2017