July 25 – 26, 2024
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
*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
ISO 13485:2016 Overview and Country-Specific Medical Devices Regulations: Six-Course Bundle
Post-Market Surveillance and Vigilance Requirements for Manufacturers (EU 2017/745)
Deviation Investigations and CAPA