Project evaluation and product objective
We analyze the idea, its technical requirements and the markets where it will be sold.
What does this service include?
COFEPRIS (Mexico): Compliance and sanitary procedures.
FDA (United States): Regulation, documentation and required processes.
From formulation, testing and design to the final production of the supplement.
Full alignment with COFEPRIS and FDA requirements to avoid delays or penalties.
Processes and tests that meet national and international standards.
Files, technical sheets, specifications and quality records.
Agile processes with expert consulting to accelerate market launch.
From the product concept to formal commercialization.
We analyze the idea, its technical requirements and the markets where it will be sold.
Scientific development, stability tests, permitted ingredients and functional design.
Files, technical sheets, labels and requirements demanded by COFEPRIS or FDA.
Procedures, validations, document submissions and regulatory follow-up.
Final production under quality standards and auditable processes
Formulation, testing, design, technical documentation and final product manufacturing.
Yes. We advise, prepare documentation and follow the entire process.
Yes. We review regulations, labeling, permitted ingredients and documentation requirements.
It depends on the supplement type and regulatory procedures, but we optimize each stage to speed up the process.
Yes. We design full product lines or supplement families for phased or simultaneous launches.
Yes. We align labeling, claims and materials with what COFEPRIS and FDA allow.
Compliance, control and preparation for market launch.
Sales