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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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Proposal to introduce a Unique Device Identification (UDI) system for medical devices in Australia
Closed on 18 February 2019
Potential reclassification of active medical devices for diagnosis and patient therapy
Closed on 18 February 2019
Medical device cyber security
Closed on 14 February 2019
Proposal for the regulation of IVD companion diagnostics
Closed on 14 December 2018
IMDRF consultation: Unique Device Identification system
Closed on 12 October 2018
IMDRF consultation: Terminologies for categorised adverse event reporting
Closed on 12 October 2018
IMDRF consultation: Principles of labelling for medical devices and IVD medical devices
Closed on 12 September 2018
Discontinuing pre-market evaluation of Herbal Component Names (HCNs)
Closed on 12 January 2018
Proposed regulatory changes related to personalised and 3D printed medical devices
Closed on 22 December 2017
Alignment with European medical device regulatory framework
Closed on 25 August 2017