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.
