The Conduct of Clinical Trials for Medicinal Products in Europe in the Light of the European Clinical Trials Directive. Review of Regulatory and Practical Aspects in the Different Countries
Thérapie 2007 May-June; 62(3): 193-197, 199-202
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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)