Cecile joined ESPL in June 2025. She is a pharmacist, and has about 8 years of experience in the pharmaceutical industry, including 5 years in regulatory affairs consultancy. Cecile is a senior regulatory consultant and medical writer, and has supported a number of pre-approval procedures (e.g., ODDs, PIPs, ILAPs, PRIME) and MA submissions. She particularly enjoys the science and the strategy behind regulatory affairs, and loves the variety of projects that working for a consultancy brings.