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Compliance with required Food and Drug Administration (FDA) regulations is easier than you may think!
This course will provide a “how to” guide for implementation of the FDA GMP requirements in the 21 CFR (Code of Federal Regulation) Part 111. These FDA regulations effect ALL companies involved with the manufacturing, packaging, labeling, and holding of dietary supplements.
Topics include methods of botanical identification, terminology included within this code, and the necessary documentation to support the packaging and quality control of botanical dietary supplements. Examples of required documentation records will be discussed and generic templates for this documentation will be provided. Each student will prepare an herbal tincture following GMP procedures and documentation.
Instructors: Sarah Schober & Chris Reedy
Note: this class takes place from 10 am to 4 pm on February 16 & 17,
in the Technology Commercialization Center (TCC), room 112
When
Thursday, February 16, 2012 at 10:00 AM
- to -
Friday, February 17, 2012 at 4:00 PM (ET)
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Where
A-B Tech, Enka Campus
1463 Sand Hill Road
Candler,
NC 28715
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