NSF-DBA GMP Course Set for December
November 30, 2011
SALT LAKE CITYNSF-DBA Dietary Supplements will provide an in-depth review of GMP (good manufacturing practice) guidelines and provide case-studies involving recent FDA warning letters for non-compliance in a course set for Dec. 7 to 8 in Salt Lake City.
The course, "21 CFR 111 Dietary Supplement GMP Overview," promises to provide a comprehensive review of FDA's Code of Federal Regulations Title 21, Part 111 [Current Good Manufacturing Practices in Manufacturing, Packaging, Labeling or Holding Operations for Dietary Supplements], providing an explanation of each subpart relevant to a companys operations. Trainers will interpret each subpart and explain how to apply the principles to an employee's or companys specific situation.
The class also offers an opportunity for discussion among the course attendees on best practices and addressing quality issues. NSF-DBA Dietary Supplements said a significant proportion of the course time will be devoted to group work, where delegates have the opportunity, through case studies, to put theory into practice.
The seminar is designed for quality and technical professionals from a variety of QA/QC, manufacturing, engineering, regulatory affairs and compliance, laboratory and other key personnel. NSF-DBA Dietary Supplements noted as a part of maintaining compliance to 21 CFR 111, dietary supplement personnel must have GMP training on a regular basis. A certificate of attendance will be provided upon completion of the course.
NSF-DBA Dietary Supplements , along with the United Natural Products Alliance (UNPA) and the National Center for Natural Products Research (NCNPR) at the University of Mississippi, also offers the program, The Dietary Supplement Quality Professional Training" (DSQP), designed for dietary supplement quality and technical professionals.
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