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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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January 06, 2012 |
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Center for Professional Innovation & Education (CfPIE), Los Angeles, CA
June 4 – 6, 2012
This course is designed for Clinical Research Monitors (CRMs), Clinical Research Auditors and others who need basic and expanded knowledge in FDA and ICH regulations for Good Clinical Practices (GCPs). This three-day program will provide attendees with the training needed to improve clinical trials and ensure compliance with Good Clinical Practice, FDA Regulations, EU Directives and ICH Guidelines. Participants will receive an in-depth understanding of the clinical research process, the roles and responsibilities of key players, and regulatory requirements.
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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=039&source=hummolgen
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E-mail:
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info@cfpie.com
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