Jan 6 2010
DBA Analytical, an NSF International company, which provides a full range of compliance services for FDA regulated industries, will host a 2-day training course on 21 CFR 111, the Current Good Manufacturing Practices (cGMPs) in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements. The seminar will be held January 27-28, 2010 at the Marriott San Francisco Airport.
The seminar enables companies to understand the GMP regulations for dietary supplements, which the US Food and Drug Administration (FDA) published in 2007. These regulations impact all manufacturers of dietary supplements who sell product in the United States. The speaker will be Dr. Norm Howe of Validation & Compliance Institute.
Compliance with the GMPs helps assure the product produced has the identity, strength, composition, quality and purity that it is represented to possess. Being audited to these requirements will help manufacturers continually improve their processes and bolster consumer confidence.
"This training reinforces NSF International's stature as a leading expert on dietary supplements," said Casey Coy, DBA's Project Manager. "We look forward to offering this relevant training to those working within the dietary supplement industry."
SOURCE Validation and Compliance Institute, LLC