Good Manufacturing Practices
The American Herbalists Guild in partnership with BioNetwork Presents:
Good Manufacturing Practices for Dietary Supplements Webinar Series
THIS SERIES WAS RECORDED IN APRIL 2015.
This webinar series provides an overview of Food and Drug Administration (FDA) current good manufacturing practice (cGMP) requirements per 21 CFR (Code of Federal Regulations) part 111. These regulations affect ALL companies involved with the manufacturing, packaging, labeling and holding of dietary supplements. This series serves as an orientation or refresher for those working in the industry.
This webinar series is presented in 4 Sessions, covering the following topics:
- Terminology and overarching concepts
- Proper documentation, including master manufacturing records (MMRs), batch process records (BPRs), standard operating procedures (SOPs), and more
- Specification requirements, which are essential for verifying that products meet the requirements set for identity, purity, strength, and composition
- Botanical identification requirements, including gross organoleptic analysis, macroscopic analysis, microscopic analysis, chemical analysis, and other scientifically valid methods
Cost for this invaluable training is only $100.00 for AHG Members, or $125.00 for the general public.
(Members must be logged in to receive discount. Discount will be applied after you add to cart.)