Guideline on virus safety evaluation of biotechnological investigational medicinal products

We have adopted this International Scientific Guideline - EMEA/CHMP/BWP/398498/2005

Last updated

29 August 2024

About this guideline

Overseas effective date: 1 February 2009

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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