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Document 32017L1572
Commission Implementing Directive on GMP for human medicinal products
Directive (UE) 2017/1572 de la Commission du 15 septembre 2017 complétant la directive 2001/83/CE du Parlement européen et du Conseil en ce qui concerne les principes et lignes directrices relatifs aux bonnes pratiques de fabrication pour les médicaments à usage humain (Texte présentant de l'intérêt pour l'EEE. )
- Legal basis:
- 32001L0083 - A47
- EuroVoc thesaurus:
- qualité du produit; rapprochement des législations; médicament; marché unique; norme de commercialisation; législation pharmaceutique; santé publique
-
- Documents:
- Ares(2017)203200 (Draft directive)
- Legal basis:
- 32001L0083 - A47
- Leading service:
- Directorate-General for Health and Food Safety
- Committee:
- Standing Committee on medicinal products for human use
- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 4
- Check the status of this initiative on the Better Regulation Portal
-
- Documents:
- C/2017/6127 final (Directive)
- Leading service:
- Directorate-General for Health and Food Safety
-
- Documents:
- 32017L1572 (Directive)
- Date of publication:
- 16/09/2017