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EAS’ popular Good Manufacturing Practices for Dietary Supplements Compliance Seminar has just been announced for April 4-5, 2018 in beautiful downtown Denver, CO. Instructed by Senior Director for Dietary Supplement and Tobacco Services, Tara Lin Couch, Ph.D., EAS Independent Advisor for Quality and Compliance, Robert Fish and Partner at the law firm Rivkin Radler, LLP, Marc Ullman, this is a dynamic opportunity to gain a deeper understanding of GMP requirements, how to develop and update action plans to meet and exceed those requirements as well as FDA’s approach to inspections.

Though the GMPs dictated in 21 CFR 111 have been in place for over a decade, FDA continues to issue numerous Warning Letters for a failure to comply with even the basic tenants of the regulation. Out of 483 inspections conducted in 2015, the agency issued approximately 290 Warning Letters. In light of increased FDA oversight, a thorough review of new industry rules on good manufacturing practices (GMPS) is warranted.

Earlybird rates are in effect through February 15, 2018. Sign up today!

Posted in EAS in Action.