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FDA issues final guidance on postmarket medical device cybersecurity

Photo of Anna Rudawski (US)
By Anna Rudawski (US) on January 5, 2017

On December 28, 2016, the U.S. Food and Drug Administration (FDA) released final guidance on the management of cybersecurity vulnerabilities for marketed and distributed medical devices.  The guidance establishes a risk-based approach for the reporting of medical device cybersecurity vulnerabilities to the FDA.

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Health information privacy and security: New compliance considerations in an era of increased interconnectivity – web seminar

Posted on September 30, 2015

On Tuesday, October 6, 2015, Norton Rose Fulbright attorneys Boris Segalis, Mark Faccenda and Kimberly Gold will present a health information privacy and security web seminar focused on compliance risks and obligations surrounding connected medical devices and healthcare data.

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