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.
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- Medical devices (59)
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More on consultations
Find more scheduling consultations on the Poisons Standard in our Interim decisions.
Read the details of recent consultations, submissions and decisions at the TGA Consultation hub.
Trove at the National Library of Australia has information on archived TGA consultations and reviews.
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188 result(s) found, displaying 51 to 75
- Closed onConsultationConsultation: Standard for vaporiser nicotine (TGO 110)TGA is consulting on a proposed standard for vaporiser nicotine products (e.g. nicotine e-liquids). Closing date: 31 March 2021
- Closed onConsultationConsultation: Fees and charges proposal 2021-22The TGA is seeking comments on the proposed fees and charges for the 2021-22 financial year. Closing date: 17 March 2021
- Closed onConsultationConsultation: Repurposing of prescription medicinesThe closing date has been extended until 30 March 2021.
- Closed onConsultationConsultation: Proposal to remove redundant processes for entering certain formulation information into a therapeutic goods applicationTGA is seeking feedback on a proposal to streamline how information about certain therapeutic goods formulations is entered into TGA electronic systems when seeking market approval. Closing date: 24 February 2021
- Closed onConsultationConsultation: Australian Medical Device Regulations definition of Central Circulatory System (CCS)A submission summary on the Australian Regulations definition of CCS consultation is available on our consultation hub
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - ACMS, ACCS and Joint ACMS/ACCS meetings, March 2021Proposed amendments to the Poisons Standard. Closing date: 27 January 2020
- Closed onConsultationConsultation: Potential reforms to medicinal cannabis manufacturing, labelling and packaging requirementA further update by the TGA on the proposed reforms to medicinal cannabis, labelling and packaging requirements.
- Closed onConsultationIMDRF consultation: Proposed update to document on Post-Market Clinical Follow-Up StudiesThe TGA (together with all other working group members) invite interested parties to comment on the document. Closing date: 11 December 2020
- Closed onConsultationConsultation: Proposed enhancements to adverse event reporting for medical devicesOutcome of the Proposed enhancements to adverse event reporting for medical devices consultation paper.
- Closed onConsultationConsultation: Exploring options for the introduction of an Australian Unique Device Identification (UDI) SystemThe closing date for this consultation has been extended until 24 December 2020
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - ACMS, ACCS and Joint ACMS/ACCS meetings, November 2020The Secretary invites public submissions on scheduling proposals. Closing date: 28 September 2020
- Closed onConsultationIMDRF consultation: Recognition and Surveillance of Medical Device Conformity Assessment BodiesDraft IMDRF document. Closing date: 9 May 2020
- Closed onConsultationIMDRF consultation: Competence and Training Requirements for Regulatory Authority Assessors of Conformity Assessment BodiesDraft IMDRF document. Closing date: 26 May 2020
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - Joint ACMS/ACCS meetings, June 2020The Secretary invites public submissions on scheduling proposals referred to the June 2020 meeting of the Joint ACMS-ACCS. Closing date: 22 May 2020
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - ACMS and Joint ACMS/ACCS meetings, June 2020Consultation extension. Closing date: 18 May 2020
- Closed onConsultationConsultation: Scope of Regulated Software based productsThe TGA is seeking feedback for the Scope Regulated Software based products. Closing date: 13 May 2020
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - Joint ACCS/ACMS meetings, March 2020The Secretary invites public submissions on scheduling proposals referred to the March 2020 meeting of the Joint ACMS-ACCS. Closing date: 10 February 2020
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - ACCS, ACMS and Joint ACMS/ACCS meetings, March 2020The Secretary invites public submissions on scheduling proposals referred to the March 2020 meetings of the ACMS, the ACCS, and the Joint ACMS-ACCS. Closing date: 10 February 2020
- Closed onConsultationConsultations on adoption of European Union guidelines in AustraliaConsultation on proposed adoption or non-adoption of EU and ICH guidelines. Closing date: 7 Feb 2020
- Closed onConsultationConsultation: Export of therapeutic goods from AustraliaThe TGA is seeking comments from interested parties on an update to guidance for the Export of therapeutic goods from Australia.
- Closed onConsultationConsultation: Review of the regulation of certain self-testing IVDs in AustraliaThe closing date of this consultation has been extended. Closing date: 6 December 2019
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - ACMS and Joint ACCS/ACMS meetings, November 2019The Secretary invites public submissions on the scheduling proposals referred to the November 2019 meetings of the ACMS and joint ACCS/ACMS. Closing date: 17 October 2019
- Closed onConsultationConsultation: Products used for and by people with disabilitiesTGA is seeking comments on clarification of the regulation of products used for and by people with disabilities. Closes: 25 October 2019
- Closed onConsultationIMDRF consultation: Good Regulatory Review Practices - Requirements for Conformity Assessment BodiesDraft IMDRF document. Closing date: 3 October 2019
- Closed onConsultationConsultation: Proposed changes to medical device essential principles for safety and performanceThe TGA is seeking comments on the proposed changes to the essential principles for safety and performance of medical devices. Closing date: 17 October 2019