The Center for Professional Advancement, Burlingame, CA
July 23-24, 2007
Who Should Attend: This course will benefit 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.
Course Type: A Two-Day Intensive Course
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