Our sister blog, The Health Law Pulse, has just blogged on the first reported instance of anti-malware causing of a medical device failure. Medical device manufacturers may wish to keep this type of interruption in mind when considering the U.S. Food & Drug Administration’s past guidance regarding the need to balance cybersecurity safeguards and the usability of the medical device in its intended environment of use.
For more information about this incident, please read the post by our colleagues Mark Faccenda and Blake Walsh.
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