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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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August 30, 2011 |
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Center for Professional Innovation & Education (CfPIE), King of Prussia, PA
Nov. 7 & 8, 2011
This course will be of benefit to pharma, medical device, and biotech professionals who manage documents for all therapeutic product development and marketing activities (including pre-clinical, clinical, QA, and regulatory functions). This two-day course is also valuable for QA auditors who need to understand what constitutes sound documentation and documentation management. Upon completion of this course participants will be able to increase your ability to implement efficient practices that meet full GLP/GMP/ICH, ISO, and other 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=027&source=hummolgen
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E-mail:
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info@cfpie.com
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