Commission Delegated Regulation (EU) 2017/1569 of 23 May 2017 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections (Text with EEA relevance. )
Basic information
Dates Date of document:
  • May 23, 2017
Date of publication:
  • September 16, 2017
Date of effect:
  • January 1, 1001
    • Application - See Art 27
  • October 6, 2017
    • Entry into force - Date pub. +20 See Art 27
Modified by
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Public health
  • Internal market - Principles
  • Testing
  • Proprietary medicinal products
  • Medicinal product
  • Bio-ethics
  • Health protection
  • Market approval
  • Health control
  • Medical research
  • Experiment on humans
  • Research and technological development
  • Medicinal products