ALEXANDRIA, Va., Jan. 24, 2019 /PRNewswire/ -- The Good Manufacturing Practices (GMP) dictated in FDA's 21 CFR 111 require that "Each person engaged in manufacturing, packaging, labeling, or holding, or in performing any quality control operations, must have the education, training, or experience to perform the person's assigned functions." In order to maintain compliance with this requirement most companies require that employees attend an annual GMP refresher training, ensuring a deeper understanding of how to perform specific job responsibilities in a GMP compliant manner.
EAS Consulting Group, LLC is offering four one-day GMP Refresher Trainings in 2019. Located around the country, these courses provide a detailed overview of expectations and compliance requirements to help employees stay on top of critical issues pertaining to GMPs. They are designed to simplify your annual GMP refresher training requirements in an in-person setting, providing an opportunity to learn directly from our GMP experts and ask specific questions regarding their GMP issues or situations.
EAS One-day GMP Refreshers are a great way to outsource your quality department's training including members of the management, regulatory affairs, and quality control/assurance teams. Join us at one of our upcoming events taught by our internationally recognized compliance experts and gain a greater understanding of your requirements under FDA's 21 CFR 111.
Dates, Locations and Instructors
- May 7, 2019 in Denton, TX – Robert Fish, Independent Advisor for Quality and Compliance
- May 14, 2019 in Riverside, CA - Timothy Stewart, Ph.D., Independent Advisor for Dietary Supplements
- August 13, 2019 in Andover, MA – Tamika Cathey, Independent Consultant
- November 12, 2019 in Plainview, NY – Heather Fairman, Independent Consultant
About EAS Consulting Group
EAS Consulting Group continues 55 plus years of leadership in providing regulatory consulting to the industries regulated by FDA and other federal and state agencies. Our network of independent advisors and consultants enables EAS to provide comprehensive consulting, training and auditing services to the dietary supplement, pharmaceutical, food, medical device, tobacco and cosmetic industries. Whether the need is assistance with general FDA or USDA regulatory compliance or more specific needs such as product development, New Dietary Ingredient submissions, FSMA regulation compliance, generic or customized compliance trainings, 483 responses, product market withdrawals or recalls, mock-FDA audits, expert witness services, GRAS & food additive issues, dietary supplement labeling compliance or the development of a detailed import strategy and policy, EAS, with its over 150 consultants, former FDA compliance officials and industry experts, is able to assist. With vast expertise in FDA's policies and enforcement, EAS is the proven choice for assistance in FDA and other regulatory matters. For more information on our GMP services visit our website at easconsultinggroup.com or contact Tara Lin Couch, Ph.D., Senior Director for Dietary Supplement and Tobacco Services at 571-447-5500.
SOURCE EAS Consulting Group, LLC