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Robert J. Morton, Jr., M.S. serves as Exelar Medical's Senior Consultant in Regulatory and Quality Assurance matters. A Board-certified Medical Physicist with nearly 30 years of relevant experience, Bob is President of Quality and Regulatory Services, Inc. (QRS). He provides our team with in-depth and expert guidance concerning 510K device clearance and other FDA requirements and brings with him a wealth of medical device commercialization experience as well.
Prior to founding QRS in 1994, Bob was Manager, Regulatory Affairs and then Director, Quality Systems and Regulatory Affairs for Siemens Medical Systems - Oncology Care Systems. He was responsible for advising the cognizant Siemens Senior Executive (now Group Vice President, SMS/OCS) and his Staff on compliance with U.S. Food and Drug Administration (FDA) regulations, including Good Manufacturing Practices, for all medical devices and devices producing electronic product radiation.
From February 1985 to February 1989, Bob was Program Director and Project Officer in the Radiotherapy Development Branch, Radiation Research Program of Division of Cancer Treatment, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
From September 1978 to May 1983, Bob was Chief of the Radiation Therapy Branch, Office of Training and Assistance Center for Devices and Radiological Health (Formerly Bureau of Radiological Health) U.S. Food and Drug Administration. Bob was FDA's Acting Deputy Director, Division of Professional Practices, Office of Training and Assistance Center for Devices and Radiological Health before joining the National Cancer Institute in 1985. | 