Law360, New York (January 15, 2016, 7:45 PM ET) — The U.S. Food and Drug Administration on Friday published detailed guidance on how medical device makers should ensure the cybersecurity of approved products and report any post-approval fixes, marking the agency’s latest move on digital threats to patients.
The draft document builds on guidance in 2014 about preapproval considerations for cybersecurity, as well as a 10-year-old guidance about medical devices For the full article click here
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