Health regulation

• Processing of health records of NEW drugs, molecules and generics.
• Review and integration of Dossier for new drug registration applications.
• Analysis and opinions of non-infringement of patents for registration of generic drugs before COFEPRIS.
• English-Spanish translation of medical and research literature for the integration of  Dossier or answering requirements.
• Lobbying to submit medicines to the Health Sector catalog and to Basic Tables.
• Pharmaco-economics studies.
• Management of notices of operation and import permits before COFEPRIS.
• Legal consultancy for preventions, extensions, and authority requirements.