• Integration and assembly of dossiers for medicines, medical devices, food supplements, food, beverages and other products for human use and consumption.
    • Preparation, integration and authorization of advertising projects by COFEPRIS.
    • Labeling of products for human use and consumption.
    • Development and monitoring of preclinical and clinical research protocols, as well as, bioequivalence and bioavailability.
    • Process and obtain certification of good manufacturing practices and sanitary licenses.
    • Support in pharmacovigilance, technosurveillance and quality management systems.
    • Integration of value arguments for the New Molecules Committee (Cofepris).
    • Obtaining sanitary authorizations such as import and export permits.