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    UNDERSTAND FDA GUIDELINES AND FTC RULES ON ADVERTI 2016 - How the FDA & FTC Regulate Advertising & Promotion of Drugs & Dietary Supplements - By Compliance Global Inc

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    Website https://complianceglobal.us/product/700412/NormaSkolnik/How-the-FDA-and-FTC-Regulate-Advertising-and | Want to Edit it Edit Freely

    Category Education; E-Learning

    Deadline: August 18, 2016 | Date: August 18, 2016

    Venue/Country: online webinar, U.S.A

    Updated: 2016-07-20 13:24:16 (GMT+9)

    Call For Papers - CFP

    Overview:

    This webinar will cover FDA regulatory compliance training requirements for all manufacturers and distributors who want to advertise and/or promote OTC drugs list and dietary supplements in the U.S. The relationship between FDA and the FTC will be covered.

    Why Should You Attend:

    In order to market dietary supplements and OTC drugs in the U.S.A., it’s essential to understand FDA guidelines and FTC rules and regulations and guidelines for advertising and promotion and to comply so as to avoid any regulatory problems.

    Areas Covered in this Webinar:

    Learn about the role of the National Advertising Division (NAD)

    Review the types of regulated advertising and promotion (TV, radio, internet ads, print ads, etc.) and regulatory requirements

    Learn how to avoid getting FDA and FTC Warning Letters

    Learn about competitive challenges

    Learning Objectives:

    Understand the relationship of FDA and FTC in regulating consumer advertising

    Understand what product claims are acceptable for advertising and promotion of dietary supplements and OTC drugs

    Who Will Benefit:

    Regulatory Affairs Managers

    Directors and Associates

    Compliance Specialists

    Marketing Managers

    Advertising Agency Representatives

    For more information, please visit : https://complianceglobal.us/product/700412/NormaSkolnik/How-the-FDA-and-FTC-Regulate-Advertising-and-Promotion-of-Drugs-and-Dietary-Supplements/1

    Email: supportatcomplianceglobal.us

    Toll Free: +1-844-746-4244

    Tel: +1-516-900-5515

    Level:

    Beginner

    Speaker Profile:

    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 as Associate Director of Marketed Product Support for Lederle Laboratories and Associate Director of Regulatory Affairs for Wyeth.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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