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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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- Remove Medical devices/IVDs filter Medical devices/IVDs (55)
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- (-) Remove Safety of medicines & medical devices filter Safety of medicines & medical devices
- (-) Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG)
- (-) Remove Medical devices safety filter Medical devices safety
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- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
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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 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
IMDRF consultation: Good Regulatory Review Practices - Requirements for Conformity Assessment Bodies
Closed on 3 October 2019
IMDRF consultation: Personalised Medical Devices - Regulatory Pathways
Closed on 24 July 2019
Proposed medical device classification for human cells, tissues and organs storage solutions and IVF media
Closed on 29 April 2019