1. FDA should further integrate its review of cybersecurity into the premarket review process for medical devices Publication: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2018 Subject(s): Computer SecurityDevice Approval -- standardsEquipment and Supplies -- standardsEquipment Safety -- standardsComputer Communication Networks -- standardsGuidelines as TopicSoftware -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
