FDA RELEASES DRAFT GUIDANCE ON POSTMARKET MANAGEMENT OF CYBERSECURITY IN MEDICAL DEVICES | McDermott

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FDA RELEASES DRAFT GUIDANCE ON POSTMARKET MANAGEMENT OF CYBERSECURITY IN MEDICAL DEVICES

June 2016

Read time: 2 min

Overview

Vanessa Burrows, Jennifer Geetter, Daniel Gottlieb and Michael Ryan wrote this bylined article analyzing FDA draft guidance addressing cybersecurity vulnerabilities in medical devices. The authors warned that “if a device manufacturer does not take steps to remediate an uncontrolled risk that is essential to its clinical performance … the FDA will consider such devices to be in violation of the [Food Drug and Cosmetics Act] and subject to enforcement action.”

Authors

Michael W. Ryan

Socio

Washington, DC

Jennifer S. Geetter

Socio

Washington, DC

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