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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 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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- Remove Prescription medicines filter Prescription medicines (7)
- 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 (3) Apply Therapeutic goods regulation filter
- (-) Remove Safety of medicines & medical devices filter Safety of medicines & medical devices
- (-) Remove Medicinal cannabis filter Medicinal cannabis
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
- (-) Remove Legislation filter Legislation
- (-) Remove Fees/Payments filter Fees/Payments
- (-) Remove Prescription medicines filter Prescription medicines
Fees and Charges Proposal 2022-23
Closed on 7 March 2022
Adoption of International Scientific Guidelines in Australia
Closed on 20 February 2022
Discussion paper on potential for mandatory reporting of medical device adverse events by healthcare facilities in Australia
Closed on 13 December 2021
Consultation on Draft Guidance: Assistive Technologies and the Therapeutic Goods (Excluded Goods) Determination 2021
Closed on 22 October 2021
Proposed refinements to the regulation of medical devices that are substances introduced into the human body via a body orifice or applied to the skin
Closed on 13 August 2021
Proposed refinements to the regulation of personalised medical devices
Closed on 14 July 2021
Remaking of standards and legislative instruments for human cell and tissue (HCT) products, blood and blood components
Closed on 11 July 2021
Proposed improvements to the Therapeutic Goods Advertising Code
Closed on 18 June 2021