Posted on
in Presentations
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.
Pre-Requisites: Familiarity with medical devices and their use within the clinical environment; familiarity with the medical device regulatory environment.
Technology Infrastructure & Operations Policy & Government Product Security
risk & vulnerability assessment operational technology (OT Security) incident response government regulations critical infrastructure
Topic
Technology Infrastructure & Operations
Policy & Government
Product Security
Subtopic
risk & vulnerability assessment
operational technology (OT Security)
incident response
government regulations
critical infrastructure
Share With Your Community