EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines #leading #pharmaceutical #companies #2013


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European Commission
Public health

EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines.

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 Directive 2003/94/EC, and 91/412/EEC respectively.

Introduction

  • Introduction (33 KB) (7/02/2011)
  • Commission Directive 2003/94/EC. of 8 October 2003, laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human use
    Replacement of Commission Directive 91/356/EC of 13 June 1991 to cover good manufacturing practice of investigational medicinal products.
  • Commission Directive 91/412/EEC of 23 July 1991 laying down the principles and guidelines of good manufacturing practice for veterinary medicinal products.

Part I – Basic Requirements for Medicinal Products

Part II – Basic Requirements for Active Substances used as Starting Materials

Part III – GMP related documents

Annexes





Last Updated on: April 21st, 2017 at 7:33 pm, by


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