Myriam Dahani

Myriam Dahani is currently the Regulatory Affairs Senior Specialist within European Global Regulatory Affairs Team at Santen Company. In her role, Myriam provides regulatory expertise for development of medical devices, and also managing regulatory aspects for the transition from MDD to MDR for Santen medical devices. Myriam has relevant experience of 8 + years in the Regulatory Affairs domain. 

She graduated as Pharmacist PhD (Paris Sud- XI University), holds a Master degree of Public Health (University of Paris V) and a statistician's diploma (Pierre and Marie Curie University – Paris).

Prior to her current role, Myriam worked for 5 years at ANSM (French National Agency for Medical Devices/Pharmaceutical Products) where she held positions in the area of Security and Vigilance, and she worked at Johnson & Johnson Company in Vigilance and Regulatory Affairs position.