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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 Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG) (1)
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- Complementary medicines (7) Apply Complementary medicines filter
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- Remove Medical devices/IVDs filter Medical devices/IVDs (55)
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- (-) Remove Listed medicines filter Listed medicines
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- (-) Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG)
- (-) Remove Medical devices safety filter Medical devices safety
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
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IMDRF consultation: Recognition and Surveillance of Medical Device Conformity Assessment Bodies
Closed on 9 May 2020
Proposed amendments to the Poisons Standard - ACCS, ACMS and Joint ACMS/ACCS meetings, March 2020
Closed on 10 February 2020
Proposed amendments to the Poisons Standard - Joint ACCS/ACMS meetings, March 2020
Closed on 10 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 amendments to the Poisons Standard - ACMS and Joint ACCS/ACMS meetings, November 2019
Closed on 17 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