Celine Bouriez

Celine Bouriez is a seasoned Regulatory and Clinical Affairs Manager at DIAGAST since November 2020, leading the IVDR compliance program and managing regulatory submissions across Europe, the USA, and globally, with expertise in Clinical Affairs and post-market surveillance. Prior to this role, Celine served as a Regulatory Affairs Project Manager at GENFIT, focusing on MAA and NDA preparations, and as a Senior Regulatory Affairs Pharmacist at SERB Specialty Pharmaceuticals, where responsibilities included product integration and M&A due diligence. Celine's earlier experiences include regulatory roles at Delpharm, LFB, and a residency at Afssaps, complemented by a Doctor of Pharmacy degree from Université de Bordeaux, a Master's in Health Law from Paris-Sud University, and a Bachelor's in science from Sainte Marie grand Lebrun.