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About Us
- Our People
- Career Opportunities
Product Experts In
Services
Our Work
Insights
- Media
- Podcasts
- Events
- Webinars
- Newsletter
- Case Studies
- Press Releases
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Blog
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Finished Product Specifications (FPS) are the foun

Finished Product Specifications (FPS) are the foundation of Natural Health Product (NHP) compliance in Canada.

Every NHP must meet strict quality standards for identity, potency, purity, microbial limits, and stability. These details are captured in the FPS and submitted to Health Canada as part of the product licence application.

Why does this matter?

✔️ Regulatory compliance – FPS prove your product meets Health Canada’s safety and quality requirements.

✔️ Quality assurance – FPS confirm consistency across every batch before it reaches consumers.

From vitamins to herbal remedies, an accurate FPS ensures products are safe, effective, and ready for market.

Need support developing compliant specifications? Visit our website or contact us at info@sourcenutra.com.

#NHPCanada #NaturalHealthProducts #RegulatoryCompliance #HealthCanada #NHPQuality

🎉 Exciting news! After joining SNI over a year

🎉 Exciting news! After joining SNI over a year ago to cover a leave, Mahsa Monshi is now officially a permanent part of our team as a Regulatory Affairs Specialist.

Her expertise, dedication, and positive energy have made her an incredible asset, and we are thrilled to have her with us full-time! 💼✨

#TeamSNI #RegulatoryAffairs #CareerGrowth #WomenInSTEM #SNICommunity #WorkplaceSpotlight

Clinical trials for natural health products (NHPs)

Clinical trials for natural health products (NHPs), including vitamins, probiotics, and herbal remedies, add scientific strength to traditional health claims.

In Canada, the approach is shifting. Sponsors are moving away from isolated studies and focusing on strategic research plans that combine feasibility assessments with clinical trial portfolio reviews.

✅ Feasibility assessments identify which products are worth studying and highlight evidence gaps that need to be addressed.

✅ Portfolio assessments look at the bigger picture by showing how individual studies work together to support regulatory submissions, expand health claims, and strengthen market opportunities.

This coordinated strategy reduces risk, saves time, and builds the type of evidence that regulators and consumers can trust.

📩 Ready to plan smarter clinical trials? Visit sniclinic.com or email us at info@sourcenutra.com to learn more.

#NaturalHealthProducts #ClinicalResearch #NHPCanada #EvidenceBased #RegulatoryCompliance

🦻Getting a medical device licensed in Canada is

🦻Getting a medical device licensed in Canada is rarely straightforward. The process is detailed, time-consuming, and one small error can hold your product back.

One of the biggest pitfalls? Misclassification. When devices are placed in the wrong class, applications are rejected. That means re-submissions, higher costs, and months of delay before you reach the market.

If you are preparing to launch a medical device, getting the classification right is the first step to success. Our latest guide breaks down Health Canada’s medical device classes so you can move forward with confidence.

🌐 Learn more on our website, or reach out to us at info@sourcenutra.com for expert, tailored support.

#MedicalDevices #HealthCanada #MedicalDeviceLicensing #RegulatoryCompliance #MedTechCanada

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