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Document 32017L1572
Commission Implementing Directive on GMP for human medicinal products
Směrnice Komise (EU) 2017/1572 ze dne 15. září 2017, kterou se doplňuje směrnice Evropského parlamentu a Rady 2001/83/ES, pokud jde o zásady a pokyny pro správnou výrobní praxi pro humánní léčivé přípravky (Text s významem pro EHP. )
- Legal basis:
- 32001L0083 - A47
- EuroVoc thesaurus:
- jakost výrobku; přibližování legislativy; léčivý přípravek; jednotný trh; tržní zvyklosti; farmaceutická legislativa; zdraví veřejnosti
-
- 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