At NutraLab Canada Corp., our 25 years of contract manufacturing leadership rests on stringent regulatory compliance, full batch auditability, and internationally recognized facility licensing. We provide complete documentation packages required by customs authorities, retail buyers, and regulatory agencies across North America, Europe, Asia, and the Middle East.
Issued by Health Canada under the Natural Health Products Regulations (NHPR). Authorizes commercial encapsulation, tablet compression, liquid filling, powder blending, and primary packaging under Canadian drug-grade standards.
Certified Good Manufacturing Practices ensuring strict SOP protocols, cleanroom air filtration, validated sanitation procedures, and full lot-by-lot batch control from raw materials to final release.
Registered under US FDA Food Facility Registration guidelines and compliant with the Foreign Supplier Verification Program (FSVP) for smooth import and clearance into the United States marketplace.
Licensed under the Canadian Food Inspection Agency (CFIA) for food safety preventative control plans, enabling international food and natural health export authorization.
Audited and certified by the Islamic Society of North America (ISNA). Verifies zero cross-contamination with non-halal agents and full ingredient traceability for Muslim-majority markets.
Rigorous ingredient verification for Kosher (Kashruth) compliance as well as non-GMO, vegan, and vegetarian formulations across capsules, tablets, liquids, and powders.
NutraLab Canada maintains active memberships and regulatory compliance with major North American natural health product associations.
For international supplement importers, obtaining clear regulatory documentation is critical to preventing customs delays and ensuring retail listing compliance. NutraLab Canada provides a comprehensive suite of verified certificates with every commercial production order.
Every lot is delivered with a full CoA detailing ingredient potency, microbiological limits, heavy metal screening, and physical specifications tested by qualified analytical laboratories.
Issued by Health Canada / Canadian authorities to confirm that products are legally manufactured and sold freely within Canada, facilitating customs clearance in target destination markets.
Official declaration confirming softgel gelatin and raw material sources are completely free of Bovine Spongiform Encephalopathy and Transmissible Spongiform Encephalopathy risks.
Verified documentation for markets requiring clean-label validation, non-irradiated assurances, and GMO-free compliance declarations.
Our Scarborough, Ontario manufacturing plant operates under rigorous Quality Assurance (QA) and Quality Control (QC) frameworks to ensure 100% batch-to-batch consistency.
Every batch of incoming raw material undergoes strict identity verification, purity analysis, heavy metal assays, and microbial screening before being cleared for production.
Continuous monitoring during encapsulation, tablet compression, liquid mixing, and powder blending checks fill weight variance, hardness, disintegration, and sealing integrity.
Finished goods are held in environmental quarantine until full analytical testing confirms strict adherence to finished product master manufacturing records (MMR).
Request facility credentials, licensing documentation, or a customized OEM contract manufacturing quote for your supplement brand today.