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.
Use the filters below to narrow your search.
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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)
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266 result(s) found, displaying 101 to 125
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Consultation: Proposed changes to Required Advisory Statements for Medicine Labels (RASML): Triptans
ConsultationOutcomes of the consultation and submissions received have now been published -
ConsultationOutcomes of the consultation and submissions received have now been published
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ConsultationOutcomes of the consultation and submissions received have now been published
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ConsultationThe outcome of the Listed medicines ingredient low-negligible risk changes 2021-22 have been published
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ConsultationThe public consultation for the Proposed refinements to the requirements for medical device patient information materials.
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ConsultationThis consultation is for interim decisions made in relation to applications and delegate initiated proposals to amend the Poisons Standard, following advice sought at the 17-18 March 2021 meetings of the Advisory Committee on Medicines Scheduling (ACMS) and Advisory Committee on Chemicals Scheduling (ACCS).
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ConsultationSubmissions published and summarised as part of a consultation on medical devices that are substances for introduction into the body.
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ConsultationThe closing date has been extended and now closes on 14 July
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ConsultationThe TGA is seeking feedback on a proposal to remake some of the legislative instruments relating to human cell and tissue (HCT) products (including blood and blood components), which sunset in October 2021. Closing date: 11 July 2021
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ConsultationThe outcomes of the public consultation into proposed improvements to the Therapeutic Goods Advertising Code have been published.
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ConsultationProposed amendments to the Poisons Standard. Closing date: 4 June 2021
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ConsultationProposed amendments to the Poisons Standard. Closing date: 27 May 2021
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ConsultationProposed amendments to the Poisons Standard. Closing date: 27 May 2021
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ConsultationProposed amendments to the Poisons Standard, including substances in hand sanitisers. Closing date: 27 May 2021
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ConsultationThe closing date for this consultation has been extended until 27 May 2021
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ConsultationThe TGA is seeking feedback on proposed advisory statements for OTC medicines containing methyl salicylate for inclusion in RASML. Closing date: 18 May 2021
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ConsultationOutcomes of the consultation and submissions received have now been published
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ConsultationOutcomes of the consultation and submissions received have now been published
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ConsultationOutcomes of the consultation and submissions received have now been published
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ConsultationView the outcomes of public consultation on building a more robust medicine supply
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ConsultationThe IMDRF working group is seeking comments from interested parties on the proposed guidance document. Closing date: 19 April 2021
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ConsultationTGA is seeking comments on whether the Australian medical device regulatory framework should be aligned to the EU framework for medical devices containing nanomaterials. Closing date: 9 April 2021
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ConsultationTGA is consulting on a proposed standard for vaporiser nicotine products (e.g. nicotine e-liquids). Closing date: 31 March 2021
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ConsultationThe closing date has been extended until 30 March 2021.
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ConsultationThis consultation is to obtain feedback in relation to proposals to provide clarity on residual claims for disinfectants. Closing date: 26 March 2021