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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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Call for further submissions on an interim decision to amend the current Poisons Standard in relation to melatonin
Closed on 28 August 2020
Notice of interim decisions on proposed amendments to the Poisons Standard - ACMS/ACCS/Joint ACMS-ACCS meetings, March 2020
Closed on 9 July 2020
IMDRF consultation: Competence and Training Requirements for Regulatory Authority Assessors of Conformity Assessment Bodies
Closed on 26 May 2020
Proposed amendments to the Poisons Standard - Joint ACMS/ACCS meetings, June 2020
Closed on 22 May 2020
Proposed amendments to the Poisons Standard - ACMS and Joint ACMS/ACCS meetings, June 2020
Closed on 18 May 2020
Scope of Regulated Software based products
Closed on 13 May 2020
IMDRF consultation: Recognition and Surveillance of Medical Device Conformity Assessment Bodies
Closed on 9 May 2020
Proposed amendments to the Poisons Standard - ACCS, ACMS and Joint ACMS/ACCS meetings, March 2020
Closed on 10 February 2020
Proposed amendments to the Poisons Standard - Joint ACCS/ACMS meetings, March 2020
Closed on 10 February 2020
Export of therapeutic goods from Australia
Closed on 3 February 2020