Explore the critical landscape of medical device cybersecurity in this 38-minute conference talk from BSidesLV 2015. Delve into key insights from Beau Woods and Scott Erven as they discuss the state of medical device cyber safety. Learn about the FDA's premarket review process, engagement strategies, and upcoming developments in the field. Gain understanding of FDA regulations, communication protocols with medical device manufacturers, and the importance of safety alerts. Discover the role of the Center for Devices and Radiological Health (CDRH) and engage with thought-provoking questions on this crucial topic. Connect with the speakers via Twitter for further dialogue on medical device cybersecurity.
Overview
Syllabus
Introduction
Suzanne Schwartz
CDRH
Key takeaways
Premarket review
FDA engagement
Whats coming
Questions
Twitter
FDA regulations
Followup dialogue
Communication with medical device manufacturers
FDA alert
FDA safety communication
Taught by
BSidesLV
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