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 126 to 150
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard - ACMS meeting, July 2016Consultation on delegate-initiated scheduling proposals - ACMS meeting July 2016. Closes 6 May 2016
- Closed onConsultationConsultation: Draft clinical evidence guidelines - Medical devicesConsultation on draft guidelines. Closing date: 10 June 2016
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard (Codeine)Further consultation on proposed changes to the scheduling of codeine. Closing date: 29 January 2016
- Closed onConsultationConsultation: Proposed amendments to Poisons Standard - ACCS and ACMS meetings, November 2015Consultation on proposed amendments to the Poisons Standard. Closing date: 29 October 2015
- Closed onConsultationConsultation: Proposed amendments to the Poisons Standard, ACMS meeting, November 2015Consultation on proposed amendments to the Poisons Standard. Closing date: 3 September 2015
- Closed onConsultationConsultation: Invitation for public comment - ACMS meeting, July 2015Invitation for public comment - proposed amendments to the Poisons Standard. Closing date: 9 July 2015
- Closed onConsultationConsultation: Proposed performance requirements and risk mitigation strategies for HIV testsConsultation on HIV self-tests. Closing date: 30 January 2015
- Closed onConsultationConsultation: Software as a medical device (IMDRF working group)IMDRF consultation. Closing date: 31 May 2014
- Closed onConsultationConsultation: Software as a Medical Device (IMDRF Working Group)IMDRF consultation. Closing date: 27 May 2015
- Closed onConsultationConsultation: Supply of in vitro diagnostic devices for self-testing (home testing) for the presence of human immunodeficiency virus in AustraliaConsultation on IVDs for self-testing. Closing date: 6 May 2014
- Closed onConsultationConsultation: Regulation Impact Statement: Changes to premarket assessment requirements for medical devicesConsultation on draft RIS. Closing date: 3 June 2013
- Closed onConsultationConsultation: Proposed amendments to the new regulatory framework for In Vitro Diagnostic medical devices (IVDs)Consultation on proposed amendments to regulatory framework. Closing date: 7 June 2013
- Closed onConsultationReview of the arrangements for the scheduling of medicines and poisons
- Closed onConsultationConsultation: Loratadine and desloratadine: proposed advisory statements for medicinesConsultation on proposed advisory statements. Closing date: 7 December 2012
- Closed onConsultationConsultation: Fexofenadine and loperamide: proposed advisory statements for medicinesConsultation on proposed advisory statements. Closing date: 4 June 2012
- Closed onConsultationReforms in the medical devices regulatory frameworkConsultation on discussion paper. Closing date: 17 December 2010
- Closed onConsultationTGA communications and consultation processes: Online survey 2009
- Closed onConsultationDraft guidance on the regulation of custom made medical devices
- Closed onConsultationUse of third party conformity assessment bodies for medical devices supplied in Australia
- Closed onConsultationRegulation of hypoxic therapy and altitude training devices (hypoxicators) in Australia
- Closed onConsultationMedical device & conformity assessment standards orders
- Closed onConsultationUpdated medical device & conformity assessment standards orders
- Closed onConsultationPublic access to information contained in ARTG entries for therapeutic goods
- Closed onConsultationRegulation of new excipients in topical non-prescription medicines
- Closed onConsultationA proposed new model for the scheduling of medicines and poisons within the Joint Agency