dicentra

🚨 Health Canada updated the NHP MAP New 12-month eligibility rules, updated PLA requirements, and changes to review prioritization. NHP applications must align with near-term Canadian market activity. Read more: buff.ly/tBpXItK #HealthCanada #NHP #RegulatoryUpdate

🚨 Regulatory Update for Canada’s food industry CFIA has updated the SFC licensing process with: 📋 New FSSI questionnaire 🔎 Expanded licence reviews ⏳ Processing timelines up to 70 business days Early renewal planning is now critical. Learn more: buff.ly/ak54B8Q

🤖 AI is already shaping regulated decisions—from claims monitoring to literature scanning ISO/IEC 42001 introduces the first global management system standard for AI governance Here’s what it means for regulated industries: buff.ly/K91HHyE #AI #ISO42001 #AIGovernance

🦠 Many probiotic trials fail because they’re underpowered. Sponsors often overestimate effect size and underestimate variability, placebo response, diet, and adherence. Learn the most common sample size mistakes: buff.ly/2FwNOFt #Probiotics #ClinicalTrials

🦠 Designing a probiotic trial? Many studies fail because the endpoint doesn’t match the claim or biology of the product. Learn how to choose endpoints that produce defensible results: buff.ly/cftR82q #Probiotics #ClinicalTrials

🍄 Functional mushrooms in foods? GRAS isn’t automatic. Species, extraction method, dose & intended use all matter. Before launching that beverage or snack, make sure your safety position is solid. Read more: buff.ly/t5Cir2N #GRAS #FDA #FunctionalMushrooms

🚨 Peptides in food? GRAS isn’t automatic. Status depends on source, manufacturing, exposure & safety data. Developing a peptide ingredient? Get the regulatory strategy right. Read more: buff.ly/Enxt0pD #Peptides #GRAS #FDA

Health Canada has abolished the Foreign Site Reference Number #FSRN process for NHPs. Foreign #GMP evidence must now be submitted through the site licensing pathway, and foreign warehouses will no longer be listed on licences. Read what this means: buff.ly/QVSr6FB

🚨 Updated Online NHP GMP Training — Now Live Fully rewritten to align with Health Canada’s updated GMP guidance (March 4, 2026). Inspection-ready training starts here: buff.ly/GKfCCH3 #NHP #GMP

#Prebiotics #NHPs #RegulatoryUpdate

🚨 Health Canada Consults on Draft Prebiotics Monograph 🚨 NNHPD has opened a 15-day consultation on a draft Prebiotics Monograph for NHPs, proposing rules for ingredients, claims, dosing, and labelling. 🗓️ Feedback due Feb 20, 2026 🔗 buff.ly/6zRmwLe

As the year wraps up, a big thank you to our clients, partners, friends, family, and colleagues for an incredible year. Wishing you a relaxing holiday season and a great start to the New Year. 🎄✨

📢 Health Canada releases two new NHP regulatory tools: the Monograph Combination Guide and List of Interchangeable Terms. These updates clarify Class II vs III submissions and offer more flexible, compliant labelling. Full update: buff.ly/ZyDW4Ru #NHP #HealthCanada

📢 Health Canada has delayed NHP cost recovery fees beyond Dec 2025. The proposal will be revisited after new regulatory reforms. Get the full update and what it means for your business ⬇️ buff.ly/E5dJ0YM #HealthCanada #NHP #Compliance

🚨 Health Canada finalizes GMP Guide for NHPs (v4.0). New requirements for quality, QAP approval, and traceability take effect March 4, 2026. 📖 Full details: buff.ly/oTelByG #HealthCanada #GMP #NHP #Compliance #Quality

📊 New on the blog: A roadmap for point-of-care diagnostics. From analytical validity to clinical utility, discover how an integrated framework streamlines studies, strengthens submissions, & speeds approvals. 👉 buff.ly/3rlG67b #POC #Diagnostics #ClinicalResearch

💄 Selling cosmetics in Canada? You must file a Cosmetic Notification Form (CNF) within 10 days of sale. Recent changes: online submissions, stricter validation, & mandatory Canadian importers. Full breakdown 👉 buff.ly/SlJK0DP #Cosmetics #HealthCanada #Compliance

🚨 FDA bans Red 3 for foods & ingestible drugs. Ingredient firms must act: identify affected products, verify replacement options, and prepare petitions if needed. Deadlines → 2027 (foods), 2028 (drugs). 👉 buff.ly/ciwZ5X3 #FDA #Red3 #FoodIngredients #Supplements

Missed our GLP-1 webinar? Watch it on demand! 🎥 Learn how to innovate responsibly in the GLP-1 space while staying compliant in Canada, the US & Europe. Watch now: buff.ly/92K1SXQ #GLP1 #Supplements #ClinicalTrials #Regulatory

🚨 Last Chance! 🚨 Our GLP-1 Inspired Supplements webinar is today at 1 PM ET. Still a few spots left! Join live to learn how to innovate responsibly in the US, Canada & EU. 🔗 buff.ly/KAhcEbd #GLP1 #Supplements #Webinar #RegulatoryAffairs #ClinicalResearch