Integral, technical, and professional advice regarding the structure of the dossiers and the obtaining of Sanitary Registers of medical devices and drugs (generic, vitamin, and herbal) before the Federal Commission for the Protection against Sanitary Risks (COFEPRIS), as well as Notices of Operation, Sanitary Licenses, Advertising and Import Permits, and Export Certificates, which are necessary in activities related to manufacturing, distribution, supply, conditioning, and sale of health supplies.
Implementation of Quality Management Systems and audits, among others.