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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.
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Referral of proposed amendment to the current Poisons Standard to the meeting of the ACMS, March 2019
Closed on 31 October 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
Referral of proposed amendments to the current Poisons Standard to the ACMS, Joint ACCS-ACMS or ACCS meeting, November 2018
Closed on 28 September 2018
IMDRF consultation: Principles of labelling for medical devices and IVD medical devices
Closed on 12 September 2018
Proposed Schedule 3 substances to be added to Appendix H of the Poisons Standard
Closed on 9 July 2018
Proposed amendments to the Poisons Standard being referred to the June 2018 meetings of the ACCS, ACMS and Joint ACCS/ACMS
Closed on 10 May 2018
Proposed Amendments to the Poisons Standard - ACCS, ACMS and Joint ACCS-ACMS meetings, March 2018
Closed on 2 February 2018
Proposed regulatory changes related to personalised and 3D printed medical devices
Closed on 22 December 2017
Proposed amendments to the Poisons Standard - ACCS, ACMS and Joint ACCS/ACMS meetings, November 2017
Closed on 6 October 2017