Vironova Biosafety
Our focus is on quality

GLP Compliance

Vironova Biosafety operates in compliance with OECD GLP guidelines and is included in the regular inspection plan of the Swedish Board for Accreditation and Conformity Assessment (SWEDAC). As stated in ICH Q5A, manufacturers of biologics are required to prove the viral removal and/or inactivation efficacy in their manufacturing process, and viral clearance studies are required to be performed in compliance with GLP principles.

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