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View this presentation for information on:
- how the manufacture of therapeutic goods is regulated
- how the quality of therapeutic goods is checked
- differences for higher, medium and lower risk products
- inspections of manufacturers, both in Australia and internationally
- international harmonisation.
*Large file warning: Attempting to open large files over the Internet within the browser window may cause problems. It is strongly recommended you download this document to your own computer and open from there.
- Regulating the manufacture of therapeutic goods (Microsoft PowerPoint,4.27Mb)*
- Regulating the manufacture of therapeutic goods (pdf,613kb)*
Disclaimer
* These educational materials are provided by the TGA (a part of the Department of Health) solely for the purpose of providing general education on the TGA regulatory scheme. The materials should not be taken to be a detailed description of the scheme, or advice on the application of the therapeutic goods legislation in particular cases. Nor should they be taken to be statements of policy.
People requiring information or advice on the application of the therapeutic goods legislation in particular cases should make their own enquiries.
Whilst due care has been taken in their preparation, the Department of Health cannot guarantee, and assumes no legal liability or responsibility for the accuracy, currency or completeness of the information contained in these materials.
These materials are based on the scheme as it is in December 2013.