Non-GMO Project Verification - Recording

It is up to dietary supplement manufacturers to ensure their supplement labels are compliant before they go to market, however the regulations can be confusing and difficult to interpret. Label noncompliance can cause your product to be considered misbranded and subject to Food & Drug Administration regulatory action.

Learn about the regulations that govern dietary supplement labeling including what can be considered a dietary supplement.

· Label compliance/noncompliance

· Regulations that govern dietary supplement

· Supplement Facts formatting

· Ingredient Lists

· Permitted claims, enforcement/litigation trends

· Adverse Event Reporting.

· The Regulatory Background and Enforcement

· Mandatory Label Elements

· Voluntary Label Elements

· How to apply the FTC and FDA regulations

· Define dietary supplement

Day 1: July 25, 2024 - 1:00 PM to 4:00 PM Eastern Time

Day 2: July 26, 2024 - 1:00 PM to 4:00 PM Eastern Time

Cost: $600.00

*Register 3 or more attendees from the same company and receive a 10% discount off each registration*

Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.

Course log in details will be sent in a separate email. Certificate of attendance will be issued upon completion of the course. Completion of the course means being in attendance 95% of the log in time

This course is 6-Hours. The labeling and promotion of your dietary supplement products are the most visible ways that the Food & Drug Administration and the Federal Trade Commission can track your compliance with federal regulations. A perfect complement to “Dietary Supplement Labeling Compliance”, this course will go over in detail each type of permitted claim that is available to you and the criteria for making each one. We will cover FDA and FTC standards for substantiation, how to build the substantiation for each claim that the FDA and FTC requires you to hold to ensure your claims are accurate and not misleading, and how you can avoid making implied claims which could lead to regulatory enforcement.
Participants will learn how public knowledge of FTC and FDA enforcement actions affect business performance, enforcement/litigation trends and other responsibilities of dietary supplement manufacturers such as structure/function claim notification.


Day: August 8, 2024 & August 9, 2024

Time: 1:00 PM to 4:00 PM Eastern Time Both Days

Cost: $600.00

*Register 3 or more attendees from the same company and receive a 10% discount off each registration*
Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.
Course log in details will be sent in a separate email. Certificate of attendance will be issued upon completion of the course. Completion of the course means being in attendance 95% of the log in time.