Heloise Mignot

Regulatory Affairs Specialist, European Medicines Agency, Netherlands

Heloise is a pharmacist with a master degree in the development of advanced therapies, biotech drugs and vaccines.
After a couple of years in the pharmaceutical industry, Heloise joined ANSM (French National Competent Authority for medicinal products and medical devices) and then MHRA (UK NCA) on the evaluation and surveillance of medicinal products, medical devices and borderlines products. For 6 years, she works at the European Medicines Agency as a Regulatory Affairs Specialist, where she now supports the implementation of the MDR/IVDR and the Committee for Advanced Therapies.