More than 10 years of experience, working in the areas of: Regulatory Affairs, Quality, Audit, Pharmaceutical Development and Laboratory, in national companies.
Experience in Quality Assurance, audits of national and foreign pharmaceutical plants, knowledge and management of National Health Legislation LGS, RIS, Regulation on Advertising, National Standards NOM-059, NOM-072, NOM-073, NOM-177, NOM-141, NOM-220 among others, International ICH legislation, SUPAC Guides, CFR 21, RTCA, PARF Network, CARPHA, EMA, PICS, among others. Knowledge of pharmaceutical manufacturing processes. Use and management of various pharmacopoeias FEUM, USP, BP, EP, JP.
Currently a student of the Master of Business Administration with a Focus on Quality and Productivity.
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