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Quality System Regulation for the Medical Device & Biotech Industries

  August 30, 2011  
Center for Professional Innovation & Education (CfPIE), King of Prussia, PA
Oct. 6 & &, 2011

This two-day course has been designed as an introductory course on the Quality System Regulation (QSR) for medical device and biotech personnel. Upon completion of this course, attendees will have gained the background knowledge necessary to understand and develop QSR compliant programs for your medical device or biotech product.  Participants will have gained insight into how to prioritize QSR implementation at each stage of development and how to assess your progress.  Attendees will also learn what the “deliverables” are at each stage of the development process.
Organized by: Center for Professional Innovation & Education
Invited Speakers: Contact info@cfpie.com for a list of course instructors
Deadline for Abstracts: n/a
Registration: http://www.cfpie.com/showitem.aspx?productid=066&source=hummolgen
E-mail: info@cfpie.com
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