Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations

Why Should You Attend:

FDA and FTC routinely initiate enforcement actions, including Untitled Letters, Warning Letters, Recalls, etc., against dietary supplement makers who misbrand their products by violating FDA advertising and promotion regulations, e.g., by claiming the product can treat, cure, prevent, mitigate or diagnose disease. Sometimes the Department of Justice gets involved and prosecutes firms on behalf of these agencies for violations. Such prosecutions often involve lawsuits against individuals running the companies, and can lead to Consent Decrees for the companies and their owners and responsible corporate officers. These threats can be avoided with proper review of promotional materials and by training and educating staff.

• Is your organization in compliance with FDA advertising and promotion regulations?
• Is FDA investigating your firm right now?
• Is your competitor blowing the whistle on you?

Learning Objectives:

At the end of this presentation, participants will

• Learn how to distinguish a violative claim from a lawful one
• Understand FDA and FTC regulations that govern what you can say about your products
• Know what to do if FDA contacts you or pays a visit
• Learn how to get started with a compliance program