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Glossary

Good PharmacoVigilance Practices (GVP) for the European Union

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A set of guidelines for the conduct of pharmacovigilance in the EU, drawn up based on Article 108a of Directive 2001/83/EC, by the European Medicines Agency in cooperation with competent authorities in the Member States and interested parties, and applying to marketing authorization holders in the EU, the Agency and competent authorities in the Member States. 

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I

International Committee for Harmonisation (ICH)

The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is…

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P

Postbiotics

Nonviable substance produced by or derived from microorganisms, which, when administered in adequate amount, confer…

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