On the market in Europe? Canada may require a novel food or food additive review, and the U.S. may call for GRAS. π¬ Our team will be at #FiEurope2026, Nov 17-19. π§
π Book a meeting with us: https://t.co/LNJpw8rRgZ #FoodIngredients
Who holds the licence when food comes into Canada: you or your importer? π
Join Drake Poirier on Dec 1 at 1:00 PM ET as he follows one shipment from order to delivery. π¦
Register π https://t.co/CT6pg1WY4k
#CFIA#FoodImport
FDA registration renewal runs October 1 to December 31. π Food facilities renew every two years. Drug and device establishments renew annually. Missing the window means filing a new registration entirely.
π https://t.co/mTr3Pn1fpr
#FDA#RegulatoryAffairs
Next stop: #FiEurope2026 in Frankfurt, Nov 17-19. πΏ Taking your ingredients to Canada or the U.S.? Let's talk Health Canada and FDA at the show. π§ͺ
π Book a meeting with us: https://t.co/uh0tCN5t3Q #FoodIngredients
DΓΌsseldorf, here we come. π Our team will be at #MEDICA2026, Nov 16-19. Bringing a medical device to Canada or the U.S.? Let's meet at your stand. π€
π Book a meeting with us: https://t.co/eghmBHnfYH #MedicalDevices
Color additives cannot qualify for GRAS status. π¨ Every new color additive for food, drugs, or cosmetics requires a formal FDA petition under 21 CFR Part 71, and commercial use cannot begin until the final rule is published.
π https://t.co/DujOvXXVqr
#FDA#ColorAdditives
That's a wrap on #SupplySideGlobal 2026! π Thank you to everyone who connected with our team in Las Vegas this week. π Missed us? Reach out to continue the conversation. π https://t.co/d0YosKKb64
Day two at SupplySide Global is in full swing! π Thanks to the clients, partners, and new connections stopping by to talk. We're here through Friday. π€ Book a time: https://t.co/CSKijjWcfW π
Andrew Parshad shares the story behind QSS on KISC My Health Radio. ποΈ From early influences to advice for future entrepreneurs. π±
Listen to the full interview. π https://t.co/lqvq9f2t92
#KISCMyHealth#Leadership
We've arrived at #SupplySideGlobal π Our team is at Mandalay Bay through Oct 30. Working on a food ingredient or supplement for the U.S. or Canada? Book a time with us π https://t.co/rlhwWlI8aA
FDA has issued a final rule allowing salt substitutes in 139 standardized foods. π§ Food manufacturers now have a clearer regulatory pathway to reduce sodium without leaving their standard of identity.
π https://t.co/5lUPEuTOKt #FDA#FoodRegulations
Health Canada confirms NHP licence holders can defer monograph-related label updates until a new transition period is set. πΏ Safety-related changes remain mandatory. Draft regulations expected spring 2027.
π https://t.co/glFth63852 #NHP#HealthCanada
#NHP application delays in Canada are preventable. πΏ Incomplete submissions, labelling gaps, and site licensing left to the end are the most common causes. Health Canada's clock only starts once your application is complete.
π https://t.co/HE0J3ULUXh
#HealthCanada
FDA has finalized NDIN guidance on identity and safety data requirements. π¬ If you're preparing a New Dietary Ingredient Notification, your dossier needs to meet a higher bar. Review your submission now.
π https://t.co/ClZCToWsDE #FDA#DietarySupplements
Tomorrow's the day. ποΈ Our live webinar on FDA's proposed mandatory GRAS rule with Andrew Parshad, Oct 20, 10 AM PT / 1 PM ET. π https://t.co/kG9vOFs8xG #GRAS#FDA
A GRAS notice requires a dietary exposure assessment covering your ingredient across the full diet. π§ͺ Without it, the FDA has no way to evaluate your toxicology data.
π https://t.co/lZbIfP7aOe
#GRAS#FDA
One formula, two markets. A U.S. dietary supplement is a natural health product in Canada, with its own licence and bilingual label π Let's talk at #SupplySideGlobal, Oct 27-30. Book a meeting π https://t.co/3LOHkXBOoj #NHP