Design and Analysis of Clinical Trials
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Who Should Participate?
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Managers, technical staff for QA and QC, and operators of pharmaceutical companies
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Managers and staff in all levels of government Food and Drug Administrations
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Administrators and researchers in medical schools, pharmacy schools, biomedical research and academic institutions
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Administrators, doctors, and nurses of clinical sites who are conducting or about to conduct clinical trials
Objectives
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To improve the skills of design and analysis of clinical trials in China and build a solid foundation in preparation for Chinese pharmaceutical products to enter the U.S. market
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To improve the acceptability of Chinese clinical trial sites in international regulatory bodies and to attract international clinical trial business to China
