Supplement Adverse Event Reports Sprout In Fertile Field Of Social Media
This article was originally published in The Tan Sheet
Compliance with FDA regulations on supplement marketers reporting serious adverse events means scrutinizing all information about a product on social media pages the same way a firm would comments that consumers or other parties submit by using contact information on product labeling.
You may also be interested in...
FTC Targets Unmasking 'Native Advertising' In Policy Update
FTC publishes enforcement policy statement addressing increases in native advertising and deceptively formatted ads. The statement explains how the commission will apply its current enforcement standards to target deceptive content, including promotions disguised as news stories, in violation of its policies.
Supplement Firms Have ‘Continuous Monitoring’ Burden To Show Product Safety
Former FDA supplement programs head Bill Frankos says the industry bears the burden for monitoring product safety in the marketplace because FDA does not have the same vested interest it has for drugs and medical devices stemming from pre-market approval of the products.
FTC Endorsement Guide Offers Refresher On Social Media Compliance Etiquette
FTC’s updated FAQ tackles questions stakeholders have been asking about its Endorsement Guide, including the appropriate way to provide disclosures on social media platforms and the responsibilities of companies using large networks of bloggers and other influencers to promote products.