From: HealthITSecurity
CHIME and AEHIS want the FDA to provide more standards for medical device cybersecurity, with more collaboration between providers and manufacturers.
More collaboration between healthcare organizations and medical device manufacturers, as well as standardized security measures are crucial to improving medical device cybersecurity, reported the College of Healthcare Information Management Executives (CHIME) and the Association for Executives in Healthcare Information Security (AEHIS).
In a recent letter, CHIME and AEHIS commented on the Food and Drug Administration’s (FDA) “Post-market Management of Cybersecurity in Medical Devices” draft, which outlines proposed regulations for identifying and managing cybersecurity risks with healthcare organizations and medical device manufacturers.
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