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Clinical Trials Legislation-Preparing for the Revision of the European Directive Scheduled for 2011

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Has the European Clinical Trials Directive been a success?

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Risk analysis and risk adapted on-site monitoring in noncommercial clinical trials

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CDISC standard-based electronic archiving of clinical trials

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Future developments of medical informatics from the viewpoint of networked clinical research

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Droit communautaire : vers une évolution de la Directive 2001/20/EC ?

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Public-private partnership models in France and in Europe

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Extended cooperation in clinical studies through exchange of CDISC metadata between different study software solutions

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European Clinical Research Infrastructures Network Meeting Report

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Developing a European framework for research on children’s medicines: an examination of the proposed EU regulation on medicinal products for paediatric use

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