Merav Yarmus

Merav Yarmus is an experienced professional in regulatory affairs, quality assurance, and clinical affairs within the medical device industry. Currently serving as VP RA, QA and Clinical Affairs at VOTIS Subdermal Imaging Technologies, Ltd., Merav is responsible for the regulatory and clinical strategies of the company, as well as the implementation of a quality management system. Previous roles include VP RA & QA at Picodya, where Merav focused on regulatory strategies and risk management, and VP Regulation at Nasus Pharma, overseeing regulatory activities for devices and combination products. Additionally, Merav held the position of VP Clinical and Regulatory Affairs at keepMED Ltd., leading regulatory strategy development and clinical studies, and worked as a clinical and regulatory consultant at BioMedical Strategy. Educational qualifications include a postdoctoral degree from the Weizmann Institute of Science and a combined MSc and PhD from The Hebrew University of Jerusalem.