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Introduction to FDA & GMP Regulations 21 CFR 210, 211
The FDA, GMP regulatory requirements and guidelines will be introduced for individuals with new positions within an FDA regulated facility. An overview of the FDA structure, function and historical development will be introduced. The federal code of regulations for 21 CFR 210 and 211 will be reviewed in detail.
- Date: August 11, 2009 (Tue), 2:30 - 4:30pm , (GMT-05:00) Eastern Time (US & Canada)
- Instructor: Sherry Davis, Quality Assurance Manager
- Rate: $90 ($65 for KOSRAP members)
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