Implementing FDA's 21 CFR 111 for Dietary Supplements

14 January 2015, Palo Alto, United States


Introduction
Although FDA's Dietary Supplement Current Good Manufacturing Practice (CGMP) Final Rule 21 CFR Part 111 has been enforced since 2010, manufacturers, distributors and importers are still not completely aware of its impact. This webinar will highlight best practices for implementing 21 CFR 111 for dietary supplements.

Why Should You Attend:
In 2007, the FDA issued the Dietary Supplement Current Good Manufacturing Practice (CGMP) Final Rule 21 CFR Part 111. Its enforcement commenced in 2010. The rule requires that proper controls be in place for dietary supplements during manufacturing, quality control, packaging, labeling, and holding and distribution. This has a high impact on manufacturers, distributors and importers of dietary supplemental products.
However, manufacturers are still uncertain about how to interpret the rule, while the FDA is preparing 483 observations and warning letters. This webinar will give attendees a good understanding of requirements for 21 CFR Part 111 and provide strategies and best practice tools for cost-effective implementation.

Note: Use coupon code 232082 and get 10% off on registration.
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Online Event, Palo Alto, Palo Alto, 94303, United States

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