Explore our turnkey private label solutions engineered to stringent cGMP safety protocols. Each product represents our commitment to raw material purity, exact active loading, and export compliance.
Premium bioactive collagen peptides for anti-aging skin beauty and joint integrity. Ultra-pure absorption profile with full regulatory traceability.
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Advanced nitrogen pump matrix engineered for vascularity, muscular endurance, and accelerated post-exercise recovery under private label branding.
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Standardized lipid signaling agent accelerating mTOR pathway activation. High stability grade ideal for sports nutrition and functional drinks.
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100% unflavored ultra-pure creatine powder. Instantized mesh size for optimal solubility and cellular ATP energy synthesis support.
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Synergistic botanical complex for male vitality, stamina, and endocrine balance. Formulated with low MOQ flexible custom packaging options.
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Tauroursodeoxycholic Acid active ingredient delivering cellular bile acid regulation and hepatic clearance support. Standardized capsule filling.
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Mineral-rich Himalayan purified Shilajit extract providing standardized 50%+ Fulvic Acid for mitochondrial bioenergetics and cellular rejuvenation.
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Essential sulfur amino acid raw material. High purity batch-tested chemical assay for pharmaceutical, nutraceutical, and dietary supplementation.
Contact UsSoftgel encapsulation relies on the precise mechanical interplay of temperature, humidity, ribbon thickness, and fill mass viscosity. As a premier Custom OEM Softgel Capsules Supplier & Exporter, NutraLab Canada utilizes state-of-the-art continuous rotary die encapsulation technology. The process begins with the thermal dissolution of pharmaceutical-grade bovine or porcine gelatin (typically calibrated to 150–200 Bloom strength) combined with plasticizers such as USP glycerine or sorbitol.
The viscoelasticity of the gel ribbon must match the hydrostatic pressure of the liquid or paste fill mass. Deviations in ribbon thickness exceeding ±0.02 mm can result in seam failure, leaking, or micro-cracking during the tumbled drying phase. Our Scarborough facility implements in-line viscometry and laser micrometer inspections to maintain structural shell integrity across various environmental conditions.
The global dietary supplement market is experiencing a structural pivot away from animal-derived softgel shells toward vegetarian alternatives. Non-animal softgels manufactured using modified tapioca starch, carrageenan, or pectin present complex engineering challenges. Plant-based hydrocolloids exhibit distinct melting points and set-up times compared to traditional collagen gelatin.
To meet this shifting demand, our R&D engineering unit has optimized low-temperature gelatinization techniques that accommodate plant-based polymer chains without sacrificing sealing force. Plant-based softgels offer enhanced thermal stability in high-humidity export climates, making them highly desirable for overseas distribution across Southeast Asia, Latin America, and the Middle East.
Softgel capsules are frequently selected to encapsulate oxidation-sensitive oils, such as Omega-3 marine oils, krill oil, evening primrose oil, and Coenzyme Q10 suspensions. Exposure to atmospheric oxygen during blending or fill prep leads to rancidity, elevated Peroxide Values (PV), and high Anisidine Values (AV).
Our Canadian manufacturing infrastructure utilizes nitrogen-blanketed mixing vessels and vacuum degassing tanks. This ensures that the Total Oxidation (TOTOX) value of marine oil formulas remains strictly below GOED (Global Organization for EPA and DHA Omega-3) guidelines (TOTOX < 26). By eliminating dissolved oxygen from the matrix prior to encapsulation, we guarantee extended shelf life and prevent unpleasant post-ingestion reflux for consumers.
Key market forces shaping contract manufacturing decisions for international importers and brand managers.
Procurement teams are prioritizing Self-Emulsifying Drug Delivery Systems (SEDDS) inside softgel shells. These micro-emulsions spontaneously form fine oil-in-water droplets upon contact with gastric fluids, drastically boosting the bioavailability of hydrophobic actives like Curcumin, Resveratrol, and Phytosterols.
Global customs authorities are enforcing stringent identity testing standards. Buyers now demand third-party analytical verification, DNA barcoding for botanicals, and heavy metal testing below micro-gram thresholds (Pb, Cd, Hg, As) before accepting shipment lots.
Targeted intestinal release softgels bypass stomach acid without requiring synthetic phthalate polymers. In-line enteric coating technology using natural alginate or shellac polymers prevents premature active degradation and eliminates fishy odor repeat.
Operating from Scarborough, Ontario, NutraLab Canada combines quarter-century technical proficiency with Health Canada site licensing.
Fully licensed facility under Health Canada Natural and Non-prescription Health Products Directorate (NNHPD). Audit-ready cGMP compliance guarantees global recognition.
Our regulatory team prepares Natural Product Number (NPN) applications, reviews label claim compliance, and generates complete Certificate of Free Sale export dossiers.
From high-speed bottling and induction sealing to blister packing, liquid filling, and powder sachets, bulk softgels never leave our controlled ambient environment.
Every production run undergoes strict raw material identity verification, microbial assay, disintegrating profile testing, and signed Certificate of Analysis (CoA) release.
Single-source convenience across Softgels, Tablets, Capsules, Liquids, Powders, and Gummies simplifies vendor qualification and unifies your product line standard.
Exporting to over 35 countries with complete customs documentation, specialized freight handling, stability protocol validation, and international compliance assistance.
Clear, definitive answers to common technical and commercial questions raised by international OEM purchasers.
Consult directly with our formula engineers and export specialists to establish batch specifications, confirm MOQ pricing tiers, and schedule sample development.
