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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries

 
  March 07, 2013  
     
 
Center for Professional Innovation & Education, Inc., Los Angeles, CA
Aug. 12 & 13, 2013


If you didn’t write it down, it didn’t happen! This is the position of the FDA and most regulatory agencies internationally.  Good documentation is vital for doing business in the regulated

world from discovery through marketplace. It is also important for due diligence and regulatory inspections, and is necessary for the success of your products and services. While the

regulations tell you what you must do, they don’t tell you how.  Based on industry best practices, this course clarifies how to refine your existing system, create a new one, or prepare to

transition from a manual system to electronic controls. 

This course also addresses what documents you need to control, what documentation you need to support your actual system and how to keep your documents current and

compliant.

 
 
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=027&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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