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Supplement OWL Progress: Mirror For Industry Support For Transparency, Mandatory Registration?

Advisory Board Members Michelson, Ramanathan Discuss Future Of VMS Registration In US

 
• By Malcolm Spicer

Advisory board for CRN-operated Supplement OWL recently reached out to industry for “ultimate reason” of recruiting participation. “Transparency has never been more important and this registry is a demonstration of this industry’s commitment to candor and honesty with our regulators, retailers and consumers,” they say.

• Source: Alamy

The Supplement Online Wellness Library may represent the transparency the US dietary supplement industry could offer consumers and that the Food and Drug Administration favors making a requirement for manufacturers and marketers.

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More from Policy & Regulation

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• By Malcolm Spicer

FDA introduced the option because it didn’t have sufficient staff to handle the volume of GRAS submission reviews requested by food and other firms for ingredients. Requiring submissions for all GRAS determinations “would just be an unworkable situation for the food industry if somehow submitting notice, submitting notices for FDA review and concurrence, was required,” says food and drug attorney Federick Stearns.

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French Agency Proposes Effective EU Ban On CBD In Foods And Cosmetics

 
• By David Ridley

France's food safety regulator ANSES is proposing a reproductive toxicity category 1B classification for CBD under the EU's CLP regulation, which would mean an effective ban on CBD in cosmetics and foods. However, French hemp industry association UIVEC hopes that new evidence coming out of a European Commission review will put the issue to bed before it gets that far.