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Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products

 
  January 15, 2014  
     
 
Center for Professional Innovation & Education, Inc., Los Angeles, CA
June 2 & 3, 2014


This course is designed to provide participants with an understanding of the parameters for regulatory compliance, successful approaches to compliance, and meeting the concerns of regulators. Attendees will leave with a comprehensive set of tools for preparing regulatory initiatives, coping with challenges, and managing compliance.

Additional benefits of this class include:

  • FDA authority and processes including 483s, Warning Letters, recalls, and other potential actions
  • The FDA electronic submission procedures
  • A chance to actively learn from fellow participants, as well as from an instructor who is a former FDA investigator and brings 20 years of practical compliance experience to a lively lecture and discussion

This course has been pre-approved by the Regulatory Affairs Professionals Society (RAPS) as eligible for 12 credits towards a participant's RAC recertification upon full completion.

 
 
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=019&utm_source=Hum-Molgen&utm_medium=Course%20Listing&utm_campaign=Web%20Listing%3A%20Hum-Molgen
E-mail: info@cfpie.com
 
   
 
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