From: CSO
The Food and Drug Administration has issued another “guidance” document on medical devices – this one devoted to keeping them secure “postmarket.”
The U.S. Food and Drug Administration (FDA) has, for the second time in two years, issued recommendations to improve the security of connected medical devices. Not mandates – recommendations.
Which immediately raises the question: Will anything that is non-binding put enough pressure on manufacturers to spend the time and money it will take to improve device security?
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