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FDA Releases Final Post-Market Guidance on Medical Device Cybersecurity


Posted on January 11, 2017 in Health Law News

Published by: Hall Render

On December 27, 2016, the Food and Drug Administration (“FDA”) issued final guidance (the “Post-Market Guidance”) outlining steps that medical device manufacturers and health care systems should take to monitor, identify, understand and address cybersecurity risks once medical devices and mobile medical devices have entered the marketplace. The Post-Market Guidance follows October 2014 FDA... READ MORE

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