CUNSA, Solution 360 - GMP Contract Manufacturing
Contract manufacturing of food supplements under GMP
We manufacture your product in a US facility that operates under FDA Good Manufacturing Practices (21 CFR Part 111). This means batch-by-batch quality control, traceability of every raw material, and auditable production documentation—the standard your international buyers and health authorities expect. You provide the brand and strategy; we take care of consistently producing what your business needs.
What is contract manufacturing?
This is the model in which a brand outsources manufacturing to a specialized producer instead of operating its own facility. You retain commercial control—brand, positioning, and distribution channels—while eliminating the investment required for infrastructure, certifications, and industrial operations. The contract manufacturer assumes technical responsibility for the formula, production process, quality, and documentation. It is the most efficient path to bringing an internationally compliant product to market without building your own manufacturing plant.
Why manufacture under US standards?
Our facility operates in compliance with 21 CFR Part 111, the FDA regulation governing dietary supplements. Manufacturing under this standard provides your product with a strong foundation for meeting the expectations of health authorities worldwide and serves as a recognized mark of quality for distributors and retail chains.
The documentation generated throughout the manufacturing process—including product specifications, batch-specific Certificates of Analysis (COAs), and GMP certification—forms the same regulatory framework that supports export activities and product registration in your target markets.
Formats we manufacture
- Capsules: The most versatile and efficient format for the majority of active ingredients.
- Softgels: Ideal for oils, fat-soluble vitamins, and sensitive active compounds.
- Powders: Suitable for proteins, high-volume blends, and higher-dose formulations.
- Sachets: Single-dose powder servings that are convenient and highly appealing on retail shelves.
Each format is supported by the appropriate quality control processes and the documentation required by your target market.
More than just producing a manufacturing partner.
The difference between a contract manufacturer and a true manufacturing partner lies in everything that surrounds the production line. CUNSA integrates formula development, regulatory adaptation, packaging design, and supporting documentation into a single project. This reduces coordination errors between suppliers and shortens the time from your idea to a product on the shelf. That is what we call our 360° Solution.
Quality and traceability in every batch
Each batch is manufactured against a defined specification and is accompanied by its Certificate of Analysis (CoA). We control the identity and characteristics of raw materials, monitor process parameters, and verify the finished product, with full traceability from the ingredient level to the final unit. If you ever need to reconstruct the history of a batch—whether for a customer inquiry or a regulatory authority—the documentation is in place and readily available.
Frequently Asked Questions
Yes. Our plant operates under the Good Manufacturing Practices for dietary supplements of 21 CFR Part 111.
Both. We manufacture formulas you already have, or we can develop them with you from scratch through our in-house Research & Development and Formulation department.
Both options. Yes. We generate Free Sale Certificates, GMP Certificates, product specifications, and batch-specific Certificates of Analysis (CoAs), among other supporting documents.
Capsules, softgel capsules, powder, and sachets.
