Celine Courtay-Cahen

Celine Courtay-Cahen has extensive experience in regulatory affairs, with a focus on gene therapy, orphan drug applications, and interactions with FDA and EMA. Celine has worked in various roles such as Senior Regulatory Affairs Manager, Regulatory Affairs Executive, and Project Manager. Celine's background includes research in canine cancers and breast cancer cell lines, as well as post-doctoral work on the cytoskeleton during the cell-cycle. Celine holds a PhD in Molecular Biology and Genomics, along with a Master's in Biochemistry.