Adam Cargill is the Vice President of Quality, Regulatory, and Clinical for MediView XR. In his role he is accountable for the oversight of all regulatory, clinical, and quality functions. Responsibilities include overseeing the company’s global regulatory, clinical, and quality strategies; provide leadership in interacting with regulatory and governmental agencies; interfacing with corporate partners to develop appropriate and compliant marketing strategies; direct the functional resources related to these areas and provide ongoing, hands-on expertise. Adam holds his BS in Psychology and Sociology, an MS in Regulatory and Clinical Affairs, is currently pursuing his Doctorate in Regulatory Science, and holds his RAC (US). He has over ten years of experience working in the medical device industry in regulatory affairs, quality, and clinical roles within orthopedic, cardiovascular, image guided therapy, radiology, ophthalmic, and augmented reality. He is the co-chair of the Industry Advisory Board of the Center for Medical Innovations in Extended Reality (MIXR) and active SME member of the Medical Device Innovation Consortium (MDIC) Medical Mixed Reality Working Group and XR Association.