Claudia Vetesi’s Post

MoFo’s Claudia Vetesi will be speaking at the ACI 12th Annual Legal, Regulatory and Compliance Forum on Dietary Supplements on June 25 in New York. Claudia will participate on the panel session “Ingredient Overages in Dietary Supplements: The Latest Compliance Concerns, Litigation Risks and Best Practices to Ensure Products Contain Declared Values Throughout Shelf-Life.” More details can be found here. https://gag.gl/ksJtHe

MoFo’s Claudia Vetesi will be speaking at the ACI 12th Annual Legal, Regulatory and Compliance Forum on Dietary Supplements on June 25 in New York. Claudia will participate on the panel session “Ingredient Overages in Dietary Supplements: The Latest Compliance Concerns, Litigation Risks and Best Practices to Ensure Products Contain Declared Values Throughout Shelf-Life.” More details can be found here. https://gag.gl/ksJtHe

Examining FDA Regulation of dietary supplements with one of the FDA leaders - Dr Cara Welch - Question - is Dr. Welch truthful and not misleading in her description of the FDA regulations and laws? What say you? What say industry? Are videos like this helpful for industry and consumers, or do they do nothing in terms of practical utility? Will lawyers use any words uttered by Dr Welch against her or the FDA or companies in any pending cases or activities? Oh, there still is no benefit to adding or giving FDA any more authorities if it does not actually do its job currently (i.e., FDA has been "complaining" about adulterated/misbranded and other issues for years), and FDA even supports Senator Durbin with his all time favorite "gas station heroin", yet since alarm bells have been raised over five years ago about this non-dietary ingredient in the US food supply (dietary supplements are regulated as a subset of foods) and the FDA has yet to take any public health safety actions (well, it has published press releases and warning letters, but no Import Alerts or prosecutions), we would say that the #FDA activities prove a Mandatory Product Listing (#MPL) will not do anything more or better or protecting public health and ensuring that the regulated marketplace stays intact. Will any company, trade association or group decide to publish consumer facing educational videos and content about the responsibilities and authorities of the FDA as a means of keeping FDA honest, or making sure the consumer can be informed? With ~70% of US citizens utilizing dietary supplements as part of their personal well-care and goals, we already know that consumers have a trust that has not appeared to waiver. Again, is Cara Welch, Ph.D. doing a service or disservice to the industry with this "educational" FDA piece? FDA Link: https://lnkd.in/eGNGd-fV #dietaryingredients #dietarysupplements #regulatory #regulatorylaw #CFR #21CFR111 #consultancy #information #parseherwords #leading #misleading #advocacy #consultant #discussion NutraIngredients Nutraceuticals World Josh Long Hank Schultz Heather Wainer PricePlow Benjamin Kane Blake Ebersole Gene Bruno, MS, MHS, RH(AHG)

https://bit.ly/3vkjmIK | We are excited to announce that we are a media partner for American Conference Institute's 12th Forum on Dietary Supplements that is taking place from June 25-26 in New York! At this year’s conference explore how the changing legal and regulatory landscape will impact current industry policies and best practices. Register today and save 10% with promo code D10-999-WF24 #DietarySupplements

This seminar starts next week! It's a thorough review of the reg with tips on practical applications and updates on regulatory enforcement. It's great for those new to the industry or if you just need a refresher!

This seminar starts next week! It’s a great comprehensive review of the regulations along with tips on actual application of those regs and updates from the agency. A great course for folks new to the industry as well as folks just looking for a solid refresher!

Question: How can I ensure my manufacturing facility meets the Current Good Manufacturing Practice (cGMP) requirements for food and dietary supplements? Consumer trust hinges on the quality and safety of food and dietary supplements. That's where Current Good Manufacturing Practice (cGMP) regulations come in. But how do you ensure your manufacturing facility meets these vital requirements? Schedule a cGMP GAP Analysis with TRE. Our experts will thoroughly assess your manufacturing processes to identify any areas that might not align with cGMP requirements. This analysis provides a clear roadmap for achieving and maintaining compliance, safeguarding your products and your business. Schedule a call here: https://vist.ly/377c2 #cGMPCompliance #FoodSafety #DietarySupplements #SupplyChainManagement #QualityAssurance

The FDA has released a new guideline on dietary supplements, finalizing Section V ('NDI Notification Procedures and Timeframes') from the 2016 revised draft guidance, along with related questions from other sections. According to Section 413(a)(2) of the FD&C Act, manufacturers or distributors of new dietary ingredients (NDIs) must submit a premarket safety notification to the FDA at least 75 days before introducing the product into interstate commerce if it hasn't been part of the food supply. It's important to note that FDA guidance documents provide recommendations and do not establish legally enforceable responsibilities unless specific regulatory or statutory requirements are mentioned. Follow us for regulatory updates and scientific insights! 💻www.toxhub-consulting.com 📩 info@toxhub-consulting.com

Consumer Health - USA/Europe/Asia Regulatory News - Feb. 2024 Stay informed on the latest health regulatory changes. Explore FDA's updates on dietary supplements, EU's ban on BPA, and Asia's guidelines for drugs and food additives. Read more: https://lnkd.in/gVqAJq75 #DietarySupplements #BPA #MedicalGuidelines #GlobalHealth #HealthcareNews #ConsumerHealthNews #RegulatoryUpdates #FDA