Harmonisation of ethics committees' practice in 10 European countries

Background: The Directive 2001/20/EC was an important first step towards consistency in the requirements and processes for clinical trials across Europe. However, by applying the same rules to all types of drug trials and transposing the Directive’s principles into pre-existing national legislations...

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Authors: Hernandez, R. (Author) ; Cooney, M. (Author) ; Dualé, C. (Author) ; Gálvez, M. (Author) ; Gaynor, S. (Author) ; Kardos, G. (Author) ; Kubiak, C. (Author) ; Mihaylov, S. (Author) ; Pleiner, J. (Author) ; Ruberto, G. (Author) ; Sanz, N. (Author) ; Skoog, M. (Author) ; Souri, P. (Author) ; Stiller, C. O. (Author) ; Strenge-Hesse, A. (Author) ; Vas, A. (Author) ; Winter, D. (Author) ; Carné, X. (Author)
Format: Electronic Article
Language:English
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Published: BMJ Publ. 2009
In: Journal of medical ethics
Year: 2009, Volume: 35, Issue: 11, Pages: 696-700
Online Access: Volltext (JSTOR)
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