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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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March 01, 2012 |
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Center for Professional Innovation & Education (CfPIE), Los Angeles, CA
July 30 & 31, 2012
This course will benefit those involved in the monitoring and/or QA of clinical trials. This two-day course will discuss some of the common issues seen in clinical trials, how to handle problem findings, and how to distinguish between poor performance and misconduct. Upon completion, attendees will be able to: Identify and define the principles and requirements for GCPs; Define the basic roles and responsibilities of the sponsor, monitor, investigators and FDA as they relate to the quality of clinical trials; understand the GCP audit process for sponsors; know when to conduct audits of vendors, sites, IRBs and laboratories and much more!
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Organized by:
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Center for Professional Innovation & Education |
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Invited Speakers:
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Contact info@cfpie.com for a list of course instructors
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Deadline for Abstracts:
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n/a
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Registration:
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http://www.cfpie.com/showitem.aspx?productid=117&source=hummolgen
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E-mail:
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info@cfpie.com
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