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WHERE THE BRIGHTEST MINDS in health and IT meet.

FDA's Final Postmarket Cybersecurity Guidance

February 20, 2017 — 01:30PM EST - 02:00PM EST
Orange County Convention Center
Booth 230|Federal Health
Session ID: 
FH05

Description

In December 2016, FDA released the final guidance, Postmarket Management of Cybersecurity in Medical Devices. The guidance articulates manufacturer's regulatory responsibility with respect to cybersecurity of medical devices that have already been cleared or approved for marketing. FDA has leveraged a risk-based framework that borrows from security-centric resources and traditional medical device risk management frameworks.

Audience: 

C-Suite

Speaker(s): 

WHERE THE BRIGHTEST MINDS

in health and IT meet.

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