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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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March 05, 2013 |
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Center for Professional Innovation & Education, Inc., Los Angeles, CA
June 3 & 4, 2013
This course will provide participants with an understanding of drug safety at the investigational stage and during the marketing phase. Adverse event identification and reporting requirements will be addressed, as well as FDA, EMA, Health Canada and ICH roles in the drug safety process. The course will also discuss international law/regulations, ICH guidelines, Pharmacovigilance, definitions and current regulatory issues.
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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=002&source=hummolgen
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E-mail:
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info@cfpie.com
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