Showing items related by title, author, creator and subject.

• Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Practice in The Conduct of Clinical Trials on Medicinal Products for Human Use 

  Unknown author (European Union. European Parliament and Council of Europe, 2001-05-01)
• Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Practice in The Conduct of Clinical Trials on Medicinal Products for Human Use 

  Unknown author (European Parliament; Council of the European Union, 2002-03)
• International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Adopts Consolidated Guideline on Good Clinical Practice in the Conduct of Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use 

  Unknown author (1997)