Uncompromising Quality Baseline
Every product batch is manufactured in accordance with validated Master Production Records (MPR). We mandate raw material identity testing via FTIR/HPLC and finished product assay testing prior to release.
Health Canada Licensed · US FDA Registered · Established 2000
About Q Nutritions — Global Nutraceutical Contract Manufacturer
Delivering science-backed formulation, rigorous quality assurance, and end-to-end CDMO services for leading supplement brands worldwide.
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Certified Quality & International Audit Standards
🇨🇦 Health Canada Site Licence
🇺🇸 US FDA Registered
✅ GMP Certified
🔬 NSF Certified
🌿 Organic Certified
☪️ Halal Certified
✡️ Kosher Certified
🛡️ HACCP
📋 ISO 22000
GMP & ISO 22000
25+ YearsOf CDMO Leadership
Corporate History & Vision
A Canadian Pioneer in Science-Driven Supplement Manufacturing
Founded in 2000, Q Nutritions has evolved from a specialized formulation laboratory into a world-class Nutraceutical Contract Development and Manufacturing Organization (CDMO). Headquartered in Mississauga, Ontario, Canada, our 50,000-square-foot flagship facility operates under stringent Health Canada Natural Health Product (NHP) regulations and US FDA 21 CFR Part 111 dietary supplement guidelines.
To support fast-growing global brands, brand owners, pharmaceutical distributors, and retail chains, we have expanded our contract manufacturing footprint with qualified production nodes and sourcing hubs in Canada, the United States, China, India, and the United Arab Emirates. We combine deep technical expertise with batch consistency so your brand can penetrate global healthcare markets effortlessly.
- 50,000 sq. ft. cGMP state-of-the-art facility
- ISO Class 8 clean room environmental controls
- Dedicated analytical QA/QC laboratory
- Full batch record traceability & retain system
- In-house PhD formulators & regulatory experts
- Global customs clearance & export documentation
Our Core Values
Built on Technical Precision, Transparency, and E-E-A-T Excellence
We serve as a reliable extension of your R&D, quality control, and supply chain management teams.
Evidence-Based R&D
Our formulations are developed by experienced pharmaceutical scientists, nutritionists, and biochemical engineers. Active ingredient overages and stability kinetics are calculated scientifically to guarantee label claim through shelf life.
Global Regulatory Expertise
Navigating cross-border compliance demands deep knowledge. Our internal regulatory team routinely files Health Canada NPN applications, US FDA label compliance reviews, EU food supplement notifications, and GCC registration dossiers.
Sustainable & Ethical Sourcing
We audit our global supply chain partners continuously for sustainable harvesting, non-GMO status, heavy metal compliance, and ethical labor standards, ensuring full material traceability from seed to shelf.
Scalable Commercialization
Whether you need pilot batch validation of 1,000 units or commercial ocean-container runs of softgels, tablets, gummies, or powders, our scalable automated lines deliver predictable lead times.
Transparent Accountability
Every client account is overseen by a dedicated Senior Project Manager. You receive complete batch documentation, Certificates of Analysis (COA), real-time production updates, and audit transparency.
Certifications & Quality Audits
Compliant with World-Leading Health & Safety Authorities
Our manufacturing sites undergo rigorous third-party audits to maintain international clearance for multi-market distribution.
Health Canada NHP
Site Licence #300459 for Natural Health Products
US FDA Registered
21 CFR Part 111 Dietary Supplement Facility
NSF International
Registered cGMP Manufacturing Standards
ISO 22000 & HACCP
Food Safety & Hazard Analysis Control System
Informed Sport / Choice
Banned-substance tested production capabilities
Halal Certified
Audited slaughterhouse & gelatine origin compliance
Kosher Certified
Strict dietary verification for qualified formulations
Certified Organic
USDA & Canada Organic certified production suites
Manufacturing Clean Rooms & Testing Labs
Advanced Infrastructure for Reliable Dosage Form Output
State-of-the-art equipment designed for high throughput, zero cross-contamination, and strict environmental stability.
In-House Analytical Quality Control Lab
Our in-house analytical testing center is equipped with High-Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma Mass Spectrometry (ICP-MS) for heavy metal trace analysis, Gas Chromatography-Mass Spectrometry (GC-MS), and automated microbiology testing suites. We analyze every raw material lot upon receipt and verify finished product potency, dissolution, and purity prior to release.
Controlled Production Clean Suites
Operating under negative/positive pressure isolation and climate-controlled humidity systems (RH <30% for moisture-sensitive probiotics and effervescents), our 11 specialized dosage suites feature high-speed rotary softgel encapsulation machines, automated tablet presses with film coating capabilities, pectin gummy cookers, and high-capacity powder blending systems.
International Supply Network
Empowering Overseas Buyers Across 40+ Destination Markets
Complete export documentation, customs assistance, and logistics tailored for global B2B buyers.
🌎 North America
Health Canada NPN registration, US FDA Supplement Facts verification, DDP & FOB shipping across Canada, USA & Mexico.
🌍 Europe & UK
EU Food Supplement compliance, EFSA claim screening, novel food status checks, and localized multi-language packaging support.
🌏 Asia-Pacific
Customs filing documentation for Japan, Singapore, South Korea, Australia (TGA awareness), and China cross-border e-commerce (CBEC).
🕌 Middle East & Africa
GCC/UAE registration dossiers, Halal certified documentation, Certificate of Free Sale (CFS), and Certificate of Origin (COO).