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GMPs for Herbs
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This workshop will introduce you to the Food and Drug Administration (FDA) current good manufacturing practice (cGMP) requirements per 21 CFR (Code of Federal Regulations) Part 111. These FDA regulations affect ALL companies involved with the manufacturing, packaging, labeling and holding of dietary supplements. Topics include: botanical identification, documentation, and terminology. More information can be found here. Date:
Saturday, March 22, 2014
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