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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
- Remove Medicinal cannabis filter Medicinal cannabis (1)
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- OTC medicines (12) Apply OTC medicines filter
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- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
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- (-) Remove Biologicals filter Biologicals
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
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- (-) Remove Disinfectants/Sterilants filter Disinfectants/Sterilants
Proposed amendments to the Poisons Standard being referred to the June 2018 meetings of the ACCS, ACMS and Joint ACCS/ACMS
Closed on 10 May 2018
Proposed Amendments to the Poisons Standard - ACCS, ACMS and Joint ACCS-ACMS meetings, March 2018
Closed on 2 February 2018
Proposed regulatory changes related to personalised and 3D printed medical devices
Closed on 22 December 2017
Proposed amendments to the Poisons Standard - ACCS, ACMS and Joint ACCS/ACMS meetings, November 2017
Closed on 6 October 2017
Alignment with European medical device regulatory framework
Closed on 25 August 2017
Proposed amendments to the Poisons Standard - Joint ACCS/ACMS meeting, July 2017
Closed on 7 July 2017
Comparable overseas regulators - medical devices
Closed on 30 June 2017
Proposed Amendments to the Poisons Standard - ACCS, ACMS and Joint ACCS/ACMS meetings, July 2017
Closed on 15 June 2017
The Scheduling Policy Framework and Advertising of Pharmacist-only medicines (Schedule 3 substances)
Closed on 28 April 2017
Accelerated assessment of medical devices - Priority Review pathway - Implementation
Closed on 11 January 2017