Guideline on the replacement of rabbit pyrogen testing by an alternative test for plasma-derived medicinal products

We have adopted this International Scientific Guideline - EMEA/CHMP/BWP/452081/2007

Last updated

27 August 2024

About this guideline

Overseas effective date: 1 November 2009

Categories: Biologicals | Active substance | Plasma-derived 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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