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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), King of Prussia, PA
July 16 & 17
This course is designed for pharmaceutical production, quality assurance, and compliance personnel who are responsible for the review and audit of production batch records, and batch record deviation investigations. The purpose of this course is to take the mystery out of the batch record review process. The class examines the FDA and EU regulatory requirements for documentation and batch record reviews, explains the elements of the batch record review process, and clarifies the pathway to effective deviation investigations.
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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=058&source=hummolgen
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E-mail:
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info@cfpie.com
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