US federal regulators have issued guidelines on preventing cyberattacks on medical devices. The Food and Drug Administration released the guidance, providing recommendations for device design, labeling, and documentation for devices with such risks. The guidance comes amidst growing concerns over recent cyber threats and older vulnerabilities in medical devices. The guidelines encourage secure product development, risk assessments, threat modeling, identification of software anomalies, and manufacturers’ responsibility in identifying cybersecurity risks.
Board-Ready Security Metrics That Actually Matter
TL;DR Board-ready security metrics translate technical capabilities into financial risk and business outcomes. Boards need visibility across three dimensions: risk exposure, incident response capability, and
