Guideline on Validation of Immunoassay for the Detection of Antibody to Human Immunodeficiency Virus (Anti-HIV) in Plasma Pools

We have adopted this International Scientific Guideline - EMEA/CHMP/BWP/298388/05

Last updated

29 August 2024

About this guideline

Overseas effective date: 1 April 2007

Categories: Biologicals | Active substance | Plasma master file

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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