To facilitate international co-operation in clinical trials on medicinal products, particularly for trials initiated by academic institutions, in December 2012 the OECD Council adopted a set of principles calling for improved consistency among national regulations and their interpretations, and on streamlined procedures for the oversight and management of clinical trials. This framework introduces a risk-based oversight and management methodology for clinical trials.
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OECD Recommendation on governace of clinical trials
Published by ECRINOrganization for economic cooperation and development (OECD)
Clinical Trials Toolkit