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GMP for Dietary Supplements

 
  January 14, 2010

Pharma Development and Business

 
     
 
CfPA - The Center for Professional Advancement, Burlingame, CA
March 11-12, 2010


Who Should Attend
This course will benefit owners, vendors, consultants and others involved in the dietary supplement industry including, but not limited to, those involved in:

  • Quality Control/Assurance 
  • Regulatory Affairs
  • Laboratory Operations 
  • Manufacturing
  • Management 
  • Labeling
  • Auditing of in-house and contract laboratories
  • Supplying and distribution of dietary supplements

Description
This two-day course will cover regulatory and legal aspects of GMP’s for dietary supplements. It will provide a comprehensive introduction and a “how to” program for implementation. Participants will understand issues involved in manufacturing and testing of dietary supplements. They will become familiar with FDA expectations when performing audits of dietary supplement companies. A rational approach to setting up manufacturing and improving a GMP compliant operation will be presented.

 
 
Organized by: CfPA - The Center for Professional Advancement
Invited Speakers: Joy Joseph; Consultant to the Pharmaceutical, Dietary Supplement and Cosmetic Industries
 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: sberg@cfpa.com
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