Commission Delegated Regulation (EU) No 357/2014 of 3 February 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council as regards situations in which post-authorisation efficacy studies may be required Text with EEA relevance
Basic information
Dates Date of document:
  • February 3, 2014
Date of publication:
  • April 10, 2014
Date of effect:
  • April 30, 2014
    • Entry into force - Date pub. +20 See Art 2
Modified by
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Proprietary medicinal products
  • Medicinal products
  • Health protection
  • Public health
  • Internal market - Principles
  • Medicinal product
  • Product safety
  • Drug surveillance
  • Market approval
  • Health control