Send us your interest if this course is currently not offered or the current schedule does not accomodate your schedule. It is often necessary to understand interest a semester in advance for planning and scheduling. Companies and organizations can often request a course if the group is large enough. This doesn't mean that we can make accommodations in every case. However, we will utilize and maximize our available resources as best as we can. Thanks for letting us know your interests and we will respond as soon as we can.
This course will provide an overview of the Food and Drug Administration (FDA) GMP 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. Examples of required documented records will be discussed and generic templates for this documentation will be provided. The last hour of class each day will be an optional Q&A session.
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