FDA Issues More Medical Device Security Guidance
New proposed cybersecurity guidance from the Food and Drug Administration is an important step in getting medical device manufacturers more focused on the risks posed by their products as they’re used in healthcare settings, security experts say.
The draft guidance on postmarket cybersecurity, issued on Jan. 15, follows the FDA’s release in October 2014 of a similar document urging medical device makers to address cybersecurity risks in the pre-market design of their products (see FDA Issues Medical Device Security Guide).
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