Description
<strong>Course Schedule - March 12-13, 2009</strong><br/><br/>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.
01/13/2009
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/2094,C8-202,0903-203.pdf
Address
Burlingame, CA USA