NÜGALE specializes in contract manufacturing for nutraceuticals, sports nutrition, natural health, pet wellness and selected cosmeceutical applications. Our capabilities include softgels and vegan softgels, two-piece hard capsules, powders, gummies, liquids, stick packs, sachets and selected topical formats.

We partner with startups, emerging brands and established national or international companies. Support can begin with a new concept, an existing formula or a product line ready to scale.

Partners receive coordinated support from concept through commercialization, backed by experienced teams, flexible manufacturing capabilities, rigorous quality systems and clear communication. Our Toronto facility is Health Canada Site Licensed and operates under GMP requirements.

Our manufacturing facility is located at 41 Pullman Court, Scarborough, Ontario M1X 1E4, Canada. It supports partners across North America and international markets.

Contact our team with your product idea, formula or current specifications. We will review your goals, target market, timing and manufacturing needs, then recommend the most suitable path forward.

Available formats include softgels and vegan softgels, two-piece hard capsules, powders and powder blends, gummies, liquids, stick packs, sachets and selected creams, lotions, gels and ointments. Final capability depends on the formula and project requirements.

Yes. We support both custom product development and private label programmes, including formulation guidance, ingredient sourcing, manufacturing, testing, packaging and commercialization support.

Our team can assist with ingredient selection, formula optimization, flavour development, stability considerations, dosage format and product specifications, with regulatory requirements considered for the intended market.

1. Consultation and project planning
2. Research and formulation development
3. Quotation and product approval
4. Ingredient and packaging sourcing
5. Manufacturing and production
6. Quality assurance and testing
7. Packaging and labelling
8. Delivery and commercialization

Minimum order quantities vary by product format, formulation complexity, ingredient availability, packaging choice and testing requirements. Our team reviews these factors with you and recommends a practical production plan for your project.

Products undergo quality assurance and testing appropriate to their specifications and applicable requirements. Testing may include ingredient identity, purity, potency and screening for heavy metals, microbial organisms and other potential contaminants.

Raw materials, packaging components and finished products are assigned lot information and documented through batch records. This supports traceability from sourcing and manufacturing through packaging and distribution.

QA and QC oversight includes raw-material inspection, in-process monitoring, equipment qualification, environmental controls, finished-product testing and production documentation under established Standard Operating Procedures.

Yes. We provide filling, labelling and finished-goods packaging across formats that may include bottles, jars, pouches, stick packs, sachets, blister packs and cartons, depending on project requirements.

We provide label review and regulatory guidance for the intended market. This may include ingredient declarations, facts panels, claims, directions, warnings and required regulatory statements. Final compliance responsibility and requirements are confirmed for each project and market.

Please provide the product format, formula or ingredient list, dosage and serving requirements, estimated quantity, packaging preferences, labelling needs, target market and desired timeline. Complete information helps us prepare a more accurate proposal and production plan.

Key factors include ingredient selection and availability, formulation complexity, dosage format, batch size, packaging and labelling, specialized processes, testing requirements, market-specific compliance and logistics.