US FDA pushed ahead with plans to enhance the agency’s approach to device cybersecurity with a two-day meeting held at agency headquarters this week to discuss cybersecurity elements that are needed in device submissions.
The meeting was organized to discuss elements of FDA’s October 2018 revised draft guidance, “Content of Premarket Submissions for Management of Cybersecurity in Medical Devices.” (Also see "Device-Makers Need To Open Up More On Cybersecurity In Pre-Market, Draft Guidance Says" - Medtech Insight, 19 October, 2018
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