Precision-Engineered Dosage Forms Built for Global Distributors, Pharmacy Chains, and Healthcare Brands in 40+ Regulated Markets.
Global Quality Baseline & Audit-Ready Standards
🇨🇦 Health Canada Site Licence🇺🇸 US FDA Registered✅ GMP Certified Facility🔬 NSF International Certified🌿 Organic Certified Line☪️ Halal Certified✡️ Kosher Certified🛡️ HACCP Compliant📋 ISO 22000 Qualified
10 Dosage Platforms
25+ YearsContract manufacturing excellence
CDMO Capabilities Overview
Commercial-Scale Supplement Manufacturing Engine
Q Nutritions is a premier Contract Development and Manufacturing Organisation (CDMO). We operate high-capacity production facilities dedicated to producing dietary supplements, natural health products (NHPs), and nutraceutical formulations that meet stringent international regulatory frameworks.
From oil-soluble active softgels to plant-based HPMC capsules, multi-layer tablets, pectin gummies, and instant powders, every dosage form is backed by rigorous analytical testing, batch-to-batch consistency, and complete regulatory dossier support for international customs clearance.
Full identity, potency & purity verification
Strict temperature & humidity-controlled cleanrooms
HPLC, GC-MS & ICP-MS analytical testing protocols
Validated allergen control & dedicated vegan lines
Certificate of Analysis (CoA) issued with every lot
Free Sale & Origin Certificates for fast export clearance
Comprehensive Product Matrix
Manufactured Dosage Forms & Delivery Technologies
Explore our validated production lines. Each format is engineered for optimal bioavailability, shelf stability, and commercial margin performance.
Softgels
Bioavailable Delivery for Lipophilic Actives
High-speed rotary die encapsulation for Omega-3 fish oils, Vitamin D3, CoQ10, MCT suspensions, and plant-based astaxanthin. Nitrogen-flushed processing minimizes oxidation, ensuring long shelf stability.
Advanced high-pressure tablet presses capable of producing dense mineral complexes, herbal extracts, and multivitamins with tight weight variation and hardness control.
• Specialties: Acid-resistant (DRcaps), delayed-release, & liquid-filled sealed hard shells.
• Standard MOQ: 50,000 units.
Functional Gummies
Consumer-Preferred Chewable Delivery Systems
Continuous starchless deposit molding lines for functional gummy vitamins. Formulated to withstand warm-climate transport without sticky degradation or active potency loss.
V-blenders and ribbon mixers engineered for homogenous distribution of micro-ingredients, protein powders, greens, collagen hydrolysates, and pre-workout drinks.
Manufactured in specialized low-humidity cleanrooms (<20% RH) to prevent premature effervescence. Rapid disintegration provides high bioavailability and refreshing taste.
Blister packing lines designed to protect sensitive active ingredients from ambient air and moisture, expanding retail shelf life and supporting consumer compliance.
• Material Types: Thermoformed PVC/PVDC film with aluminum foil or Cold-Form ALU-ALU.
• Applications: Softgels, hard capsules, compressed tablets.
• Cartoning: Automatic insertion into unit cartons with patient/consumer leaflets.
• Standard MOQ: 50,000 blister cards.
Quality & Compliance Assurance
Uncompromised Manufacturing Standards for Global Import
Every commercial production run is governed by Health Canada Natural Health Product (NHP) GMP standards and US FDA 21 CFR Part 111 rules.
Raw Material Identity
100% incoming raw material testing via FT-NIR and HPLC to confirm botanical identity, chemical structure, and supplier documentation authenticity.
Heavy Metal & Purity Testing
ICP-MS analysis verifies lead, arsenic, cadmium, and mercury levels comply with strict California Prop 65, Health Canada, and European Commission safety limits.
Microbial & Contaminant Screen
Automated pathogen screening for E. coli, Salmonella, Staphylococcus aureus, yeast, mold, pesticides, and residual solvent traces (GC-MS).
Complete Batch Records
Full batch manufacturing records (BMR) maintained for every lot, detailing line clearance, equipment logs, in-process weight checks, and yield reconciliation.
Structured Execution
The 5-Stage Commercial Production Process
A streamlined technical workflow engineered to take your supplement formulation from initial laboratory prototype to retail-ready inventory.
01
Formulation Brief
Technical evaluation of active ingredients, target dosage form, regional compliance limits, and target unit cost target.
02
Lab Bench Trials
R&D formulators test active-excipient compatibility, dissolution profiles, taste-masking, and physical stability parameters.
03
Pilot & Analytical Release
Small-scale pilot run to validate machine throughput, tablet hardness, capsule fill uniformity, and analytical testing protocol accuracy.
04
GMP Production
Scale-up into full commercial batch manufacturing under class 100,000 HVAC cleanroom conditions with continuous quality checks.
05
Final CoA & Export Release
Quality Assurance releases finished product with batch Certificate of Analysis, Free Sale Certificate, and export freight documentation.
MOQs start at 50,000 units for capsules, tablets, and softgels; 100,000 units for functional gummies and effervescent tablets; 500 kg for powder blends; and 10,000 bottles for liquid formats. Pilot batch runs are available for R&D and regulatory stability testing.
Yes. Every commercial batch undergoes rigorous identity, potency, heavy metal, microbiological, and physical parameter testing (HPLC, ICP-MS, GC-MS). Certificates of Analysis (CoA) and complete batch records accompany every international shipment.
Our in-house R&D and regulatory affairs team handles master formula design, active overage calculation, stability testing, Health Canada NPN submissions, US FDA label review, EU food supplement compliance, and GCC registration dossiers.
Yes. We offer plant-based HPMC capsules, tapioca/pectin softgels and gummies, gluten-free powder lines, and sugar-free sweetening systems utilizing erythritol, stevia, and monk fruit. Swab-tested allergen control protocols prevent cross-contamination.
Ready to Manufacture Your Custom Supplement Line?
Consult with our technical sales engineers to review formula specifications, minimum order quantities, and custom packaging options. Receive a formal quotation within 24 hours.
