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Consultations
We conduct public consultations as part of our broader stakeholder engagement work, including on changes to regulatory requirements or practices, reviews of business processes, standards or guidelines, and TGA fees and charges.
Trove at the National Library of Australia has information on archived TGA consultations and reviews.
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- Advertising (2) Apply Advertising filter
- Australian Register of Therapeutic Goods (ARTG) (1) Apply Australian Register of Therapeutic Goods (ARTG) filter
- Biologicals (2) Apply Biologicals filter
- Complementary medicines (7) Apply Complementary medicines filter
- Fees/Payments (1) Apply Fees/Payments filter
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- Listed medicines (2) Apply Listed medicines filter
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- Remove Medical devices/IVDs filter Medical devices/IVDs (55)
- Remove Medical devices safety filter Medical devices safety (1)
- Remove Medicinal cannabis filter Medicinal cannabis (1)
- Remove Medicines filter Medicines (2)
- Medicines safety (1) Apply Medicines safety filter
- OTC medicines (12) Apply OTC medicines filter
- Remove Other therapeutic goods filter Other therapeutic goods (1)
- Prescription medicines (7) Apply Prescription medicines filter
- Scheduling (56) Apply Scheduling filter
- Therapeutic Goods Administration (TGA) (2) Apply Therapeutic Goods Administration (TGA) filter
- Remove Therapeutic goods regulation filter Therapeutic goods regulation (2)
- (-) Remove Medical devices/IVDs filter Medical devices/IVDs
- (-) Remove Medicinal cannabis filter Medicinal cannabis
- (-) Remove Medicines filter Medicines
- (-) Remove Other therapeutic goods filter Other therapeutic goods
- (-) Remove Therapeutic goods regulation filter Therapeutic goods regulation
- (-) Remove Medical devices safety filter Medical devices safety
Products used for and by people with disabilities
Closed on 25 October 2019
Proposed changes to medical device essential principles for safety and performance
Closed on 17 October 2019
IMDRF consultation: Good Regulatory Review Practices - Requirements for Conformity Assessment Bodies
Closed on 3 October 2019
Proposed clarification that goods are therapeutic goods - goods containing folate substances in certain circumstances
Closed on 18 September 2019
IMDRF consultation: Personalised Medical Devices - Regulatory Pathways
Closed on 24 July 2019
Proposed new classification rule for medical devices that administer medicines or biologicals by inhalation
Closed on 29 April 2019
Proposed medical device classification for human cells, tissues and organs storage solutions and IVF media
Closed on 29 April 2019
Proposed new medical device classification for substances introduced into the body via a body orifice or applied to the skin
Closed on 29 April 2019