Sara Furie MSc is a chemist and a regulatory affairs executive and has been working in the pharmaceutical industry in regulatory affairs and clinical drug development for the past 20 years. Her broad expertise includes regulatory affairs, FDA/EMA interactions and submissions, clinical research planning and management, medical writing, GMP and support services to the pharmaceutical / medical device industries. Sara held industry positions at Teva Pharmaceutical Industries API division; Coeruleus a drug development start up company and Peflex a medical device start up. Sara is a respected speaker on topics related to life science regulatory/ quality / clinical development in Israel including Tel Aviv University School of continuing medical education and Israel export institute.