European Guidance on Clinical Trials (Extracts)
BULLETIN OF MEDICAL ETHICS 64: 13-17, December 1990
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EEC Note for Guidance: Good Clinical Practice for Trials on Medicinal Products in the European Community Unknown creator (European Economic Community. Committee for Proprietary Medicinal Products. Working Party on Efficacy of Medicinal Products, 1991)
Guidance for Industry. Using a Centralized IRB Review Process in Multicenter Clinical Trials. Draft Guidance Unknown creator (United States. Food and Drug Administration [FDA]; Good Clinical Practice Program, Office of the Commissioner [OC]; Center for Drug Evaluation and Research [CDER]; Center for Biologics Evaluation and Research [CBER]; Office of Regulatory Affairs [ORA], 2005-03)