The Australian Register of Therapeutic Goods (ARTG) is the central database of therapeutic goods that can be legally supplied in or exported from Australia.
Medical devices included in the ARTG have sponsors. These sponsors take legal responsibility for the supply of their medical devices in or from Australia.
Medical device sponsors must have their product in the ARTG unless the product is exempt or excluded.
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Stay informed
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SectionFind out the latest news and updates about the regulation of therapeutic goods in Australia, as well as events, webinars and consultations with the community.
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PageThe medical devices reforms aim to enhance the safety, performance, and quality of medical devices in Australia and focus on patient safety.
Regulatory consultants and industry associations
We do not provide details of regulatory affairs and therapeutic goods regulations consultants. Sponsors and manufacturers might find it helpful to contact a relevant industry association.
We do not endorse these associations.
- Association of Regulatory and Clinical Scientists Australia (ARCS)
- AusBiotech
- Australian Dental Industry Association (ADIA)
- Australian Self-Medication Industry Association (ASMI)
- Complementary Medicines Australia (CMA)
- Pathology Technology Australia (PTA)
- Medical Technology Association of Australia (MTAA)
- ACCORD Australasia
Providing feedback to the TGA
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PageFind out how to report an adverse event, including side effects from taking medicines and problems with medical devices.
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PageYou can access unapproved therapeutic goods in certain circumstances. Find out who can apply, what you can access and what to do before you apply.
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