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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 Therapeutic goods regulation filter Therapeutic goods regulation (2)
- (-) Remove Safety of medicines & medical devices filter Safety of medicines & medical devices
- (-) Remove Therapeutic goods regulation filter Therapeutic goods regulation
- (-) Remove Labelling/Packaging filter Labelling/Packaging
- (-) Remove Medicinal cannabis filter Medicinal cannabis
- (-) Remove Australian Register of Therapeutic Goods (ARTG) filter Australian Register of Therapeutic Goods (ARTG)
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
Regulation Impact Statement: Changes to premarket assessment requirements for medical devices
Closed on 3 June 2013
Reforms in the medical devices regulatory framework
Closed on 17 December 2010
Draft guidance on the regulation of custom made medical devices
Closed on 31 March 2009
Use of third party conformity assessment bodies for medical devices supplied in Australia
Closed on 27 March 2009
Regulation of hypoxic therapy and altitude training devices (hypoxicators) in Australia
Closed on 5 September 2008
Medical device & conformity assessment standards orders
Closed on 15 August 2008
Updated medical device & conformity assessment standards orders
Closed on 15 February 2008
Public access to information contained in ARTG entries for therapeutic goods
Closed on 3 February 2006
Draft guidelines: In vitro diagnostic goods for home-use
Closed on 1 August 2003
Labelling project 99/00 Effective by design
Closed on 23 June 2000