What The FDA’s Postmarket Management of Cybersecurity in Medical Devices Means for Manufacturers of Medical Devices
The FDA‘s guidance on “Postmarket Management of Cybersecurity in Medical Devices”[PDF] is a complementary document for the 2014’s “Content of Premarket Submissions for Management of Cybersecurity in Medical Devices” [PDF]. The 30 pages of the guidance contain detailed recommendations, and the…
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