Commission Directive 2005/28/EC of 8 April 2005 laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (Text with EEA relevance)
Basic information
Dates Date of document:
  • April 8, 2005
Date of publication:
  • --
Date of effect:
  • April 29, 2005
    • Entry into force - Date pub. + 20 See Art 32
Date of transposition:
  • January 29, 2006
    • At the latest See Art 31.1
Modified by
Repealed by:
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Approximation of laws
  • Medical research
  • Experiment on humans
  • Import
  • Medicinal product
  • Pharmaceutical legislation
  • Public health
  • Internal market - Principles
  • Health protection
  • Proprietary medicinal products