Session Details

Description

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, mandatory aspects on the principal display panel, Supplement Facts formatting, ingredient lists, and type of permitted claims, enforcement/litigation trends, and other responsibilities of dietary supplement manufacturers such as Adverse Event Reporting. The course is interactive, with hands-on exercises. Bring your questions and prepare to interact with the instructor and your peers in the industry.

This course is geared to those individuals involved in the dietary supplement industry including:

• Management                     

• Marketing

• Quality Control/Assurance        

• Packaging

• Sales                                                

• Laboratory Operations

• Product Development                                

• Suppliers and Distributors

• Regulatory Affairs                                                

• Legal

*Note: SupplySide West & Food ingredients North America registration is required to register for this course. Click here to register for this year’s event and available GMP courses.

Produced by:

• GMP and Regulatory Compliance Training Program