Bachelor’s Degree in Chemistry and Pharmacy, with 18 years of professional experience specializing in regulatory affairs, quality management, physicochemical analysis, and compliance with national and international health regulations. She has extensive experience in managing sanitary registrations for pharmaceutical products, medical devices, and chemical substances, as well as conducting audits, managing documentation, implementing Good Manufacturing Practices (GMP), and overseeing controlled substances. She has led multidisciplinary teams and coordinated regulatory processes with health authorities, ensuring compliance with technical and legal requirements. She holds postgraduate qualifications in Integrated Quality Management Systems and has experience in university-level teaching in Biochemistry and General Biology. Her professional background combines scientific rigor, quality management, analytical skills, and regulatory expertise, with a strong focus on continuous improvement, technical accuracy, and regulatory compliance.