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Eudralex Volume 4 – EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use

This document provides guidance for the interpretation of the principles and guidelines of good manufacturing practice (GMP) for medicinal products as laid down in Directive 2003/94/EC for medicinal products for human use and Directive 91/412/EEC for veterinary use, and the Clinical trials Regulation 536/2014, the Commission Delegated Regulation 2017/1569 supplementing it.

Read the news announcement published by the European Commission on 21 February 2022.


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (15 mars 2022). Eudralex Volume 4 – EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/o5wq


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