Last week, the Food and Drug Adminstration (FDA) closed the public comment period on the draft guidelines for Postmarket Management of Cybersecurity in Medical Devices.
FDA Postmarket Cybersecurity Guidance Respects Clinical Workflow
Posted by
Michael Holt on Apr 26, 2016 11:28:56 AM
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Topics: FDA, Healthcare Cybersecurity, Medical Device Security, Ransomware, Clinical Information Systems, Medical Device ePHI, Clinical Security