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About this guideline
End of consultation (overseas): 31 May 2008
Categories: Biologicals | Finished product | Investigational medicinal products
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.