Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use Text with EEA relevance
Basic information
Dates Date of document:
  • May 28, 2014
Date of publication:
  • November 25, 2014
Date of effect:
  • May 25, 2015
    • Application - See Art 19
  • December 15, 2015
    • Entry into force - Date pub. +20 See Art 19
Modified by
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Mode of production
  • Internal market - Principles
  • Public health
  • Technical specification
  • Drug surveillance
  • Quality standard
  • Proprietary medicinal products
  • Medicinal product
  • Marketing standard
  • Medicinal products