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Pharmaceutical Production Batch Record Review

 
  March 06, 2013  
     
 
Center for Professional Innovation & Education, Inc., Los Angeles, CA
June 17 & 18, 2013


This course is intended 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.  Interactive sessions are included for identifying reviewer responsibilities, establishing good documentation practices, and writing procedures for the review process.  Additionally, participants will be able to analyze their company’s compliance with these requirements and identify missing elements of the batch review 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=058&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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