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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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- Remove Complementary medicines filter Complementary medicines (7)
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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
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- Medicines safety (1) Apply Medicines safety filter
- OTC medicines (12) Apply OTC medicines filter
- Remove Other therapeutic goods filter Other therapeutic goods (1)
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- Remove Safety of medicines & medical devices filter Safety of medicines & medical devices (0)
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- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
- Therapeutic goods regulation (2) Apply Therapeutic goods regulation filter
- (-) Remove Labelling/Packaging filter Labelling/Packaging
- (-) Remove Safety of medicines & medical devices filter Safety of medicines & medical devices
- (-) Remove Complementary medicines filter Complementary medicines
- (-) Remove Other therapeutic goods filter Other therapeutic goods
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
Proposed new classification rule for medical devices that administer medicines or biologicals by inhalation
Closed on 29 April 2019
Proposed regulatory scheme for personalised medical devices, including 3D-printed devices
Closed on 31 March 2019
Proposed reclassification of spinal implantable medical devices
Closed on 31 March 2019
Regulation of software, including Software as a Medical Device (SaMD)
Closed on 31 March 2019
Proposal to introduce a Unique Device Identification (UDI) system for medical devices in Australia
Closed on 18 February 2019
Potential reclassification of active medical devices for diagnosis and patient therapy
Closed on 18 February 2019
Changes to a number of definitions and the scope of the medical device regulatory framework in Australia
Closed on 18 February 2019
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