Eric Marthinet is a Regulatory Affairs Manager with extensive experience in pre-MAA and post-MAA procedures for medicinal products. Currently at GENFIT since 2020, Eric prepares and submits regulatory documents for Centralised MAAs, Clinical Trial Applications, and various regulatory dossiers in Europe and the US. Previously, Eric has held positions at TempoPHARMA, EXCELYA, and Hays Life Sciences, where they contributed to regulatory affairs and pharmacovigilance during clinical trials. Eric’s educational background includes Clinical Research Associate training from Supsanté Lyon, complementing their professional expertise in the field.
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