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Good Clinical Practices for the Clinical Research Professional

5 May 2008, Horsham, United States


Introduction
With the goal of helping to ensure well-trained clinical investigators and study staff to conduct safe and effective clinical trials, this training course provides the basic knowledge required to conduct clinical trials, including knowledge about subject safety, regulations, and the practicalities of performing research studies. This one-day training course format is a compressed and streamlined lecture.

COURSE HIGHLIGHTS
•Roles and responsibilities of investigators, study staff, research institutions, and IRBs.
•Regulations and guidelines that govern clinical investigations.
•Practices that ensure effective and efficient study conduct.

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Venue
DIA

DIA, 800 Enterprise Rd., Suite 200, Horsham, 19044, United States

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Organised by
Drug Information Association
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