Victoria Espínola

Regulatory Affairs professional, with a Degree in Pharmaceutical Chemistry. More than 10 years of experience in Industry, with an emphasis on global CMC requirements. Expertise in planning, driving, and executing regulatory submissions and developing innovative regulatory strategies to accelerate drug access and continuous supply for patients. Current role in Roche as Regulatory Program Director in Pharma Technical Regulatory (PTR), in charge of CMC aspects of submissions to international markets. Lead of a reliance pilot for a post approval change of a biologic product (2024-2025).