How the FDA & FTC Regulate Advertising & Promotion

Event Information
Product Format
Prerecorded Event
Conference Date
Mon, Jul 24, 2017
60 minutes
Product Description

Challenges in Marketing OTC Drugs While Complying with FDA and FTC Regulations


Join this presentation with expert speaker Norma Skolnik that addresses the challenges of marketing and advertising over-the-counter (OTC) drugs and dietary supplements successfully in the U.S. She will share how this can be done while remaining in compliance with FDA and FTC regulations and avoiding Warning Letters and competitive challenges.

The presentation will help attendees understand the role of the FDA and the FTC in regulating advertising and promotion of OTC drugs and dietary supplements. It will also provide know-how tips on how to avoid trouble when advertising OTC drug and dietary supplement products. References to all relevant FDA and FTC regulations and guidance documents will be provided.

Session Highlights:

  • Understanding the relationship between FDA and FTC in regulating consumer advertising
  • Product claims that are acceptable for advertising and promotion of dietary supplements and OTC drugs will be reviewed
  • Learn about the role of the National Advertising Division (NAD)
  • Review the types of regulated advertising & promotion (TV, Radio, Internet ads, print ads, websites, etc.) and regulatory requirements
  • Learn how to avoid receiving FDA and FTC warning letters and enforcement actions
  • Learn about competitive challenges and how to handle them

Who should attend?

  • Regulatory Affairs managers & associates
  • Drug & dietary supplement marketing managers
  • OTC Drug & dietary supplement product managers
  • Consumer Healthcare business managers

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

Order Below or Call 1-866-458-2965 Today

You can also order through:




About Our Speaker

Norma Skolnik - FDA Regulations Expert

Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that, she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and...   More Info
More Events By The Speaker

Why AudioEducator?
  • Save money on travel.
  • Meet your specific training needs.
  • Keep learning after the event.
  • Save time training your whole staff.
Join Our Mailing List
Our Accreditation Partners
Facebook Twitter Linkedin Youtube RSS Feeds Google Plus
Audio Educator


Dear Valued Customers


We regret to announce that ProEdTech LLC and all its affiliate brands will cease operations on April 1, 2019.


We are no longer able to fulfill online orders. We will fullfill all DVD and book orders already placed.


Customers of canceled webinars and subscription products may request a refund at (800) 223-8720 or You must do so by April 1, 2019.


Thank you for your business and loyalty over the years. We sincerely apologize for any inconvenience caused.


Best regards,

The ProEdTech Team