Use of customer testimonials, reviews, or endorsements in the advertising of dietary supplement products can be considered “commercial speech”, depending on how and where it is used. It is the responsibility of your organization to ensure use of this content in the promotion and advertising of products is not only used with permission, but is also accurate and compliant with FDA and FTC regulations. This webinar discusses important regulatory considerations when incorporating user-generated content in the advertising of dietary supplements.
Our culture of thriving mobile technology, internet, and social media has facilitated the communication of information, allowing consumers the opportunity to share experiences and communicate with others about the dietary supplements they use. Indeed, the success and growth of many in this industry is founded on customers sharing their honest product reviews and experiences (i.e. “testimonials”).
It is important to remember, however, that testimonials and endorsements may not always be accurate and could be deceptive, dangerous, or even harmful to public health. Because this content can be considered “commercial speech”, depending on how and where it is used, it is the responsibility of your organization to ensure that all testimonials, reviews, and/or endorsements used officially by the company in the promotion and advertising of products is not only used with permission, but is also accurate and compliant.
There are several governing agencies that monitor the use of endorsements and testimonials in advertising and can take action against your company. As the advertiser, you are subject to liability for false or unsubstantiated statements made through endorsements and testimonials. This webinar has been created to help guide your company in complying with the applicable Food and Drug Administration (FDA) and Federal Trade Commission (FTC) regulations.
Learn effective strategies minimize risk when using user-generated content in the promotion and advertising of your dietary supplement.Areas Covered in the Webinar:
Director of Regulatory Affairs, Plexus Worldwide
Travis MacKay is the Director of Regulatory Affairs for Plexus Worldwide, a leading direct sales company with a range of products dedicated to helping others obtain health and happiness. He currently oversees international regulatory compliance activities driving strategic direction focused on claims development and substantiation strategy, product development and commercialization, international formulation considerations, and quality testing & validation.
Travis has 20 years of quality and regulatory experience, including prior regulatory affairs leadership positions within well-respected, global consumer product companies. He has a passion for mentoring regulatory professionals to develop robust compliance systems that keep business moving forward.
Travis Graduated from the University of Utah in 2002 with a B.S. in Behavioral Science and Health (Human Health Emphasis). He is a fly-fishing enthusiast, a college football fan, an exercise junky, and a lover of classic cars. He escapes the noise by spending time with his family in the outdoors of beautiful Arizona.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.
Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.
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