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Development and regulation of safe supplements

What does this service include?

Complete solutions for supplements

Advisory and management of regulatory permits:

COFEPRIS (Mexico): Compliance and sanitary procedures.
FDA (United States): Regulation, documentation and required processes.

Benefits

  • Complete product development

    From formulation, testing and design to the final production of the supplement.

  • Guaranteed regulatory compliance

    Full alignment with COFEPRIS and FDA requirements to avoid delays or penalties.

  • Certified quality and safety

    Processes and tests that meet national and international standards.

  • Technical and sanitary documentation

    Files, technical sheets, specifications and quality records.

  • Optimized time-to-market

    Agile processes with expert consulting to accelerate market launch.

  • Specialized support throughout the entire cycle

    From the product concept to formal commercialization.

Development process

Project evaluation and product objective

Project evaluation and product objective

We analyze the idea, its technical requirements and the markets where it will be sold.

Formulation, design and testing

Formulation, design and testing

Scientific development, stability tests, permitted ingredients and functional design.

Technical and sanitary documentation

Technical and sanitary documentation

Files, technical sheets, labels and requirements demanded by COFEPRIS or FDA.

Permit management and compliance

Permit management and compliance

Procedures, validations, document submissions and regulatory follow-up.

Production and release of the product

Production and release of the product

Final production under quality standards and auditable processes

FAQs

What does comprehensive development of a dietary supplement include?

Formulation, testing, design, technical documentation and final product manufacturing.

Do you also manage COFEPRIS permits?

Yes. We advise, prepare documentation and follow the entire process.

Can you help me comply with the FDA?

Yes. We review regulations, labeling, permitted ingredients and documentation requirements.

How fast can I launch my product?

It depends on the supplement type and regulatory procedures, but we optimize each stage to speed up the process.

Can I develop several products at the same time?

Yes. We design full product lines or supplement families for phased or simultaneous launches.

Do you support labeling and allowed claims?

Yes. We align labeling, claims and materials with what COFEPRIS and FDA allow.

Supplements that are safe, regulated and ready to compete

Compliance, control and preparation for market launch.