EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines. Introduction Replacement of Commission Directive 91/356/EC of 13 June 1991 to cover good manufacturing practice of investigational medicinal products. Commission Directive91/412/EECof 23 July 1991 laying down the principles and guidelin...
EudraLex The Rules Governing Medicinal Products in the European Union Volume 4 EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use - Part 1 Chapter 2: Personnel
Volume 4 of 'The rules governing medicinal products in the European Union' contains guidance for the interpretation of the principles and guidelines of good manufacturing practices for medicinal products for human and veterinary use laid down in Commission Directives 91/356/EEC, as amended by Directiv...
Part IV - GMP requirements for Advanced Therapy Medicinal Products EudraLex - Volume 4 (europa...
EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Consumer goods Pharmaceuticals Brussels, 14 February 2008 EudraLex The Rules Governing Medicinal Products in the European Union Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use Annex 1Manufactur...
Volume 4 of 'The rules governing medicinal products in the European Union' contains guidance for the interpretation of the principles and guidelines of good manufacturing practices for medicinal products for human and veterinary use laid down in Commission Directives 91/356/EEC, as amended by Directiv...