Consultations
Search open and closed consultations on the way we regulate medicines, medical devices and biologicals.
- You can also find, read and respond to recent consultations, submissions and decisions at the TGA Consultation hub.
- Find more scheduling consultations on the Poisons Standard in our Interim decisions.
- Archived consultations and reviews can be viewed on the National Library of Australia Trove site.
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Topic
- Scheduling (national classification system) (81)
- Legislation (15)
- Committees and advisory bodies (12)
- Labelling and packaging (7)
- Manufacturing (7)
- Safety monitoring and information (5)
- Advertising (3)
- Fees and payments (3)
- Import and export (3)
- Sunscreens (3)
- Medicinal cannabis hub (2)
- Shortages and supply disruptions (2)
- Clinical trials (1)
- Compliance and enforcement (1)
- Unique Device Identification (UDI) hub (1)
- Vaping hub (1)
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266 result(s) found, displaying 176 to 200
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ConsultationThe TGA sought comments on the proposal to introduce new and amended definitions, and a revised scope of the products regulated as medical devices in Australia. Closing date: 18 February 2019
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ConsultationThe TGA sought comments on the applicability and usefulness of the content contained in the draft regulatory guidance and information materials. Closing date: 14 February 2019
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ConsultationInvitation to comment on proposed amendments to the Poisons Standard - ACCS, March 2019 (late addition to the published agenda). Closing date: 8 February 2019
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ConsultationProposed Amendments to the Poisons Standard are now available for public comment. Closing date: 21 January 2019
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ConsultationDiscussion paper outlining different approaches to access and safety controls for alkyl nitrites
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ConsultationClosing date extended to 14 December 2018
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ConsultationAdvisory Committee on Medicines Scheduling to consider upscheduling of modified release paracetamol to 'Pharmacist Only'. Closing date 31 October 2018
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ConsultationThe IMDRF sought comments on a proposed guidance document and two information documents
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ConsultationThe IMDRF sought comments on a proposed document and its annexes
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ConsultationInvitation to comment on proposed Poisons Standard amendments. Closing date: 28 September 2018
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ConsultationThe IMDRF is seeking comments on a proposed guidance document
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ConsultationThe TGA is seeking comments on the proposed guidance for the use of Boxed Warnings for prescription medicines. Closing date: 31 August 2018
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ConsultationThe TGA sought comments on the proposed Schedule 3 substances to be added to Appendix H of the Poisons Standard to allow them to be advertised direct to consumers. Closing date 9 July 2018
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ConsultationCarbendazim has been deferred from the June 2018 ACCS meeting at the applicant’s request.
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ConsultationConsultation on options for a regulatory response to the potential misuse of prescribed Schedule 8 opioids in Australia
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ConsultationInvitation to comment on proposed amendments to the Poisons Standard. Closing date: 2 February 2018
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ConsultationConsultation on proposed process for pre-market evaluation of HCNs. Closing date: 12 January 2018
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ConsultationConsultation on future options for the regulation of personalised and 3D printed medical devices. Closing date: 22 December 2017
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ConsultationInvitation to comment on proposed amendments to the Poisons Standard - ACCS, ACMS & Joint ACCS/ACMS meetings, November 2017
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ConsultationConsultation on proposed changes to up-classify surgical mesh medical devices and to provide patient implant cards for implantable medical devices. Closing date: 25 August 2017
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ConsultationThe TGA sought comments from interested parties on the proposed amendments to the Poisons Standard. Closing date: 7 July 2017
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ConsultationConsultation on comparable overseas regulators. Closing date: 30 June 2017
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ConsultationThe TGA sought comments from interested parties on the proposed amendments to the Poisons Standard. Closing date: 15 June 2017
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ConsultationThe TGA sought comments from interested parties on the options for the future regulation of 'low risk' products. Closing date: 12 May 2017
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ConsultationOptions for the reform of the SPF and advertising controls of Schedule 3 medicines. Closing date: 28 April 2017