Consultations
We consult on proposed changes to the way we regulate medicines, medical devices and biologicals. Additional consultations about changes to the Poisons Standard can be found in the Scheduling decisions (interim) section of our publications hub.
See all open and recent consultations, submissions and decisions at the TGA Consultation hub.
More on consultations
Find more scheduling consultations on the Poisons Standard in our Interim decisions.
Trove at the National Library of Australia has information on archived TGA consultations and reviews.
Use the filters below to narrow your search.
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Topic
- Scheduling (national classification system) (76)
- Therapeutic goods regulation (18)
- Prescription medicines (15)
- Over the counter (OTC) medicines (14)
- Legislation (12)
- Complementary medicines (11)
- Non-prescription medicines (10)
- Advisory bodies and committees (9)
- Listed medicines (9)
- Labelling and packaging (6)
- Manufacturing (6)
- Medical devices safety (4)
- Advertising (3)
- Biological medicines (3)
- In Vitro Diagnostic medical devices (IVDs) (3)
- Medicines safety (3)
- Sunscreens (3)
- Australian Register of Therapeutic Goods (ARTG) (2)
- Fees and payments (2)
- Import and export (2)
- Safety (2)
- Shortages (2)
- Artificial Intelligence (AI) (1)
- Assessed listed medicines (1)
- Blood and blood components (1)
- Clinical trials (1)
- Disinfectants/Sterilants (1)
- Medicinal cannabis hub (1)
- Registered complementary medicines (1)
- Unique Device Identification (UDI) hub (1)
- Vaping hub (1)
Please use the filters or search function to help find relevant consultations.
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249 result(s) found, displaying 176 to 200
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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
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ConsultationConsultation on discussion paper. Closing date: 11 January 2017
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ConsultationConsultation on discussion paper. Closing date: 11 January 2017
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ConsultationIMDRF consultation document. Closing date: 2 December 2016
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ConsultationConsultation on the proposed amendments to the Poisons Standard. Closing date: 20 October 2016
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ConsultationThe TGA sought comments from interested parties on the proposed amendments to the Poisons Standard. Closing date: 20 October 2016
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ConsultationPublic consultation on proposed amendments to the Poisons Standard. Closing date: 24 June 2016
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ConsultationConsultation on draft guidelines. Closing date: 10 June 2016
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ConsultationConsultation on delegate-initiated scheduling proposals - ACMS meeting July 2016. Closes 6 May 2016
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ConsultationFurther consultation on proposed changes to the scheduling of codeine. Closing date: 29 January 2016
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ConsultationConsultation on proposed amendments to the Poisons Standard. Closing date: 29 October 2015
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ConsultationConsultation on proposed amendments to the Poisons Standard. Closing date: 3 September 2015
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ConsultationInvitation for public comment - proposed amendments to the Poisons Standard. Closing date: 9 July 2015
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ConsultationThe TGA sought comments from interested parties on the proposed adoption of two European Union guidelines as guidance material for sponsors and manufacturers of medicines including herbal ingredients.
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ConsultationConsultation on HIV self-tests. Closing date: 30 January 2015
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ConsultationConsultation on IVDs for self-testing. Closing date: 6 May 2014
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ConsultationConsultation on proposed amendments to regulatory framework. Closing date: 7 June 2013
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ConsultationConsultation on draft RIS. Closing date: 3 June 2013