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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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Good Clinical Practices for the Clinical Research Professional | |
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February 12, 2008 |
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Drug Information Association, DIA, 800 Enterprise Rd., Suite 200, Horsham, PA, USA
May 5 2008
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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Organized by:
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Drug Information Association |
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Invited Speakers:
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Bernie OttConsultantUnited States.
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Deadline for Abstracts:
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-
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Registration:
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http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=15840&eventType=Training%20Course
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E-mail:
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dia@diahome.org
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