Dietary Supplement Labeling Compliance Seminar
September 17-18, 2020 • Clayton, MO
Dietary supplement manufacturers need to keep up to date on new and changing FDA labeling policies as they will undoubtedly carry over to an increased focus on labeling enforcement. This seminar provides all that is necessary to prepare labels that comply with FDA requirements. It will address the regulatory requirements for the mandatory labeling elements and will cover allowable dietary supplement claims. Attendees will participate in a workgroup exercise to facilitate their understanding of the regulations as well as understand how dietary supplement label requirements differ from those of foods and issues that have triggered FDA enforcement actions.
Who Should Attend?
- Individuals involved in management, regulatory affairs, and quality control/assurance in the manufacturing of dietary supplements.
- Those responsible for preparing or reviewing supplement labels.
- Consultants, auditors, attorneys and others interested in supplement labeling compliance.
At the Dietary Supplement Labeling Compliance Seminar, You Will
- Learn FDA supplement facts panel labeling requirements from labeling experts who helped to develop and implement the current regulations and have reviewed hundreds of labels for the industry.
- Learn about hot issues that have triggered recent FDA warning letters.
- Apply learning in practical work sessions.
- Have your specific issues addressed and discussed in a casual, interactive learning environment.
- Participant’s Manual
- EAS Type Size Guide
- Food Label Handbook – Developed by EAS Independent Consultant, Gisela Leon, the 115-page guide discusses how changes to nutrient values are listed and how those changes impact claims, assisting companies in developing compliant food labels based on FDA’s final rule. (A $99 value.)
James E. Hoadley, Ph.D.,
EAS Independent Consultant
During Dr. Hoadley’s 20-year FDA career, he participated in the development of NLEA-implementing nutrition labeling and health claim regulations. As a Senior Regulatory Scientist in the Office of Nutritional Products, Labeling and Dietary Supplements (ONPLDS) Dr. Hoadley’s primary responsibilities were in food label claim regulations. In this role, he conducted scientific and regulatory reviews of petitions for new health claims and nutrient content claims.
EAS Independent Consultant
Gisela Leon brings in over 21 years of experience in international labeling of food and over 8 years’ experience in US labeling. As a regulatory consultant, she has focused on a concise review process for food, dietary supplements, and cosmetics. As a long term EAS Consultant she has reviewed hundreds of labels for US compliance and helped international products to come into compliance with US regulations. Her international labeling background allows her to point out differences or similarities with other countries.
EAS will conduct this seminar for individual firms upon request. Bringing the seminar in-house at your facilities can be a cost-effective alternative to train your employees. It also allows the program to be tailored to your particular needs. Contact Cathryn Sacra for a price quote. (571) 447-5500 or email@example.com.
$625.00 – $700.00
Group Rate, two or more from the same firm
10% per person (group10)
Federal/State Government Employees
50% per person (gov50)
In effect through July 15, 2020. Use “earlybird” to receive 10% off registration at checkout.
Registrants with Promotion codes – Limit one Promotion code per transaction
Hampton Inn & Suites Clayton/St. Louis-Galleria Area
216 N Meramec Avenue
Clayton, Missouri 63105
Hilton Garden Inn is offering a discounted guest room rate for seminar attendees. Click here to be directed to their reservations page.
Minimum Registration Policy
Should the minimum enrollment number for the seminar not be met, EAS has the right to cancel by August 10, 2020, and refund the registration fee in full.
Cancellations received before August 10, 2020 will result in a $95 processing fee. No refunds will be given for cancellations received after that date. Substitutions will be allowed as long as notice is given to EAS in advance.