Guideline on the investigation of manufacturing processes for plasma-derived medicinal products with regard to VCJD risk

We have adopted this International Scientific Guideline - CPMP/BWP/CPMP/5136/03

Last updated

20 August 2024

About this guideline

Overseas effective date: October 2004

Categories: Biologicals | Active substance / Finished product

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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