Sofia Silva is an International Regulatory Lead at Amgen, where they develop strategies and support regulatory and clinical trial filings. They previously served as a Regulatory Affairs Specialist at IQVIA and held various roles in regulatory affairs and pharmacy, including as a Regulatory Affairs Officer and Medical Writer at Grupo Medinfar. Sofia has a Master's degree in Pharmacy from Faculdade de Farmácia da Universidade de Lisboa, an MBA in Management/Health from Fundação Getulio Vargas, and further qualifications in Clinical Trials and Medical Affairs. Their extensive experience encompasses managing global regulatory projects and clinical trials across multiple pharmaceutical companies.
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