Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use (Text with EEA relevance. )
Basic information
Dates Date of document:
  • September 15, 2017
Date of publication:
  • September 16, 2017
Date of effect:
  • October 6, 2017
    • Entry into force - Date pub. +20 See Art 17
Date of transposition:
  • January 1, 1001
    • Application See Art 16.1
  • March 31, 2018
    • Adoption See Art 16.1
Modified by
Modifies
Repeal:
Affected by case
Legal basis
EuroVoc Vocabulary
  • Product quality
  • Public health
  • Internal market - Principles
  • Pharmaceutical legislation
  • Technical barriers
  • Medicinal product
  • Approximation of laws
  • Proprietary medicinal products
  • Marketing standard
  • Single market
  • Public health