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) (83)
- Legislation (16)
- Committees and advisory bodies (12)
- Labelling and packaging (9)
- Manufacturing (9)
- Safety monitoring and information (6)
- Fees and payments (5)
- Advertising (4)
- Sunscreens (4)
- Import and export (3)
- Shortages and supply disruptions (3)
- Compliance and enforcement (2)
- Medicinal cannabis hub (2)
- Clinical trials (1)
- Unique Device Identification (UDI) hub (1)
- Vaping hub (1)
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281 result(s) found, displaying 276 to 281
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ConsultationThis consultation opened on 21 December 2007 and closed on 15 February 2008.
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ConsultationThis Discussion Paper provides a basis for discussions with stakeholders regarding the proposal to publicly release therapeutic goods information in respect of Australian Register of Therapeutic Goods (ARTG) entries.
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ConsultationThis consultation opened on 28 November 2005 and closed on 16 December 2005. It remains on this website as a historical reference.
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ConsultationConsultation on proposed new model for the scheduling of medicines and poisons within the Joint Agency
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ConsultationIn July 2003, the TGA consulted on a guidelines document (below) developed by the Office of Devices, Blood and Tissues for sponsors of home-use in vitro diagnostic devices (IVDs).
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ConsultationDiscussion paper on possible reforms to the regulation of the labelling of medicines in Australia.