SQF Institute’s Post

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!

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

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on dietary supplements, finalizing Section V ('NDI Notification Procedures and Timeframes') from the 2016 revised draft guidance, along with related questions from other sections.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

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

Download the case study to decipher how Freyr assisted a leading US-based company specialized in dietary supplements with ingredient review, formulation assessment, and claims review. https://lnkd.in/gCV8nAPQ #RegulatoryServices #DietarySupplements #ProvenCase #IngredientReview #FormulationAssessment #FreyrSolutions

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

🔎 Recapturing Regulatory Hurdles: Dietary Supplements via Direct Sales 🔍 We've been diving into the compliance and regulatory challenges in the dietary supplement industry. Today, let’s focus on consumer concerns with dietary supplements sold through direct sales channels. Direct sales offer convenience, but worries about product safety, efficacy, and transparency persist. 🤔 Join us as we explore: ✔ Key consumer concerns ✔ Actionable insights for addressing them By tackling these issues, direct sales companies can build trust and foster transparency. Read the full blog post here: https://lnkd.in/gMUwhf6w. What are your thoughts on these consumer concerns? Share your insights below! 👇. #innaconsultingservices 🔔 #ConsumerConcerns #DietarySupplements #DirectSales This content is for informational and educational purposes only.

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