Présentation d'Eléonore

Hello, Advising the cross functional team from an EU regulatory perspective for the development of gene therapies indicated in rare genetic diseases. My role includes: - assess the regulatory feasibility of the planned developments and define the regulatory strategy - draft documentation for health agencies to apply for scientific advice, clinical trial authorisation, etc - coordinate interactions with cross functional team, CRO, health agencies, external partners and associations - Regulatory intelligence and policy I was able to work in various therapeutic areas and products in small biotech and large pharma companies which allowed me to gain quickly a solid background in regulatory affairs. Feel free to contact me if you want to know more about my job Eléonore