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About this guideline
Overseas effective date: 19 December 2014
Provided for information: 1 September 2015
Note: This reflection paper is intended as a supplement to the Guideline on human cell-based medicinal products (EMEA/CHMP/410869/2006)
Categories: Multidisciplinary | Cell therapy and tissue engineering
TGA Annotations: Nil
- Where EU guidelines adopted in Australia include references to EU legislation (including EC Directives and Regulations), the requirements contained in the referenced EU legislation are not applicable to the evaluation of medicines by the TGA.
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For more information see International scientific guidelines adopted in Australia.