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WHO Guideline TDR/PRD/Ethics/2000.1 – Ethics CommitteesThe purpose of this wide consultative process was to ensure extensive input while fostering the sharing of knowledge from developing and developed countries alongside organizations and institutions with varying degrees of experience and expertise. This process also help to prepare for the dissemination of the final text through an international process of capacity building that would strengthen national and local infrastructures for ethical review throughout the world.The Operational Guidelines for Ethics Committees That Review Biomedical Research are proposed by the WHO and CIOMS as a support for improving the organization, quality, and standards of ethical review around the world. These Guidelines take into ac-count current practices while suggesting guidance for a harmonized state-of-the-art approach. Comments and suggestions on all aspects of these guidelines are welcome for consideration in future revisions of this document. Please correspond with: Dr Juntra Karbwang Clinical Coordinator Product Research and Development TDR/CDS/ WHO CH-121 1 Geneva 27 Switzerland Tel (41) 22 791 3867/8 Fax (41) 22 791 4854 E-mail: karbwangj@who.ch
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