Safety Implications of Medical Device Cybersecurity


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It is critical to come to ground truth when high consequence vulnerabilities are discovered in medical devices. The FDA is exploring the development and viability of a Cyber Med Safety Analysis Board to integrate critical patient safety and clinical environment dimensions into the assessment and validation of high-risk/high-impact device vulnerabilities and incidents.

Pre-Requisites: Familiarity with medical devices and their use within the clinical environment; familiarity with the medical device regulatory environment.


Participants
Penny Chase

Participant

Information Technology and Cyber Security Integrator, MITRE

Margie Zuk

Participant

Senior Principal Cybersecurity Engineer, MITRE

Technology Infrastructure & Operations Policy & Government Product Security

risk & vulnerability assessment operational technology (OT Security) incident response government regulations critical infrastructure


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