Merav has 15+ years of experience in regulatory and clinical affairs, mainly in EU and US. Before joining Nasus Pharms Merav worked as a clinical and regulatory consultant and as VP clinical and regulatory affairs of medical device companies in diverse fields (e.g., cardiology, orthopedics, radiology, in vitro diagnostics, sleep medicine), guiding them successfully through FDA clearance, CE mark and clinical trials.

Merav obtained her PhD in molecular biology from the Hebrew University of Jerusalem, and did a post-doctorate at the Weizmann Institute of Science.