Dusica brings over 13 years of experience in Regulatory Affairs and Quality Management within the medical device industry, with deep expertise across EU MDR, UK and CH regulations, ISO 13485, risk management, and Notified Body interactions. Throughout her career, she has built and led QA/RA teams from the ground up, managing professionals across both small, agile start-ups and large multinational organizations, and working across a wide range of device technologies and device classes.