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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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Discussion paper on potential for mandatory reporting of medical device adverse events by healthcare facilities in Australia
Closes on 13 December 2021
Notice of interim decisions on proposed amendments to the Poisons Standard – Joint ACMS-ACCS #28 – June 2021
Closes on 11 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard – ACCS #31 – June 2021
Closes on 11 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard (sodium nitrite) - June 2021
Closes on 11 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard - ACMS #34 (oral contraceptive substances) - June 2021
Closes on 1 November 2021
Notice of interim decisions on proposed amendments to the Poisons Standard - ACMS #34 - June 2021
Closes on 1 November 2021