Regulator guidance
Supplying or manufacturing medical devices containing poisons
Therapeutic Goods Administration. Guideline, Australia-wide.
- Version
- Last updated 30 September 2024
- Last read
- 24 September 2026
The regulator's guidance on medical devices that contain a scheduled substance, such as dermal fillers and other injectable implants: which of them the Poisons Standard applies to, and how they are labelled.
What changed
- 20 April 2018First published 20 April 2018The page states a publication date of 20 April 2018 and a last updated date of 30 September 2024.
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