Regulatory affairs specialist
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Biotechnology engineer with over 6 years of experience, with extensive knowledge in regulation, eager to develop my management skills.
COFA INTEGRAL S.A DE C.V. Authorized chemical verifier by COFEPRIS with experience in drug medicines, biotechnological and allopathic medicines. Evaluation of legal, and technical documentation.
Productos Medix, S.A. DE C.V. Regulatory affairs chemist responsible of LATAM área, with regulation experience in Guatemala, El Salvador, República Dominicana, Paraguay, Panamá Honduras. GMP and CLV request, participation in the GMP recertification issued by COFEPRIS.
Laboratorios Eurofarma de México, S.A. de C.V. Regulatory affairs Analist Sr. Review and evaluation of legal and technical documentation focused in the obtaining of New marketing authorization, variations and renewals. Experience in New Molecules Committe, labeling, advertisements, alimentary supplements, knowledge of CTD format, ICH, Mexican regulation.
Biotechnology engineer in the Instituto Politécnico Nacional.
Diplomate in regulatory affairs of supplier for health. I AM
Regulatory affairs specialist (in Progress) UNISA-COFEPRIS
