As cybersecurity expectations tighten across the healthcare sector, organizations that develop, supply, or operate medical devices face growing pressure to improve Software Bill of Materials (SBOM) transparency and vulnerability management. Teams must go beyond generating SBOMs for compliance. They must ensure accuracy, continuously monitor risk, and respond rapidly to emerging threats.
Regulators such as the FDA and global frameworks such as the IMDRF are raising the bar. They emphasize secure product design, ongoing vulnerability management, SBOM inclusion in technical documentation, and timely communication of risks across the product lifecycle. Increasingly, this also extends to post-market surveillance and coordinated vulnerability disclosure.
In practice, these expectations require automated and operational SBOM workflows. Organizations must be able to generate complete, high-fidelity SBOMs in machine-readable, industry-standard formats, continuously monitor components against evolving vulnerability intelligence, including sources like the CISA Known Exploited Vulnerabilities (KEV) catalog, and rapidly triage, prioritize, and communicate vulnerabilities to stakeholders across the ecosystem.
In this webinar, you will learn:
• What evolving medical device cybersecurity guidance requires from both engineering teams and healthcare providers
• Practical approaches to uncover deeply embedded third-party components within firmware
• How to reduce gaps caused by incomplete SBOMs
• Ways to streamline vulnerability identification, triage, and disclosure
• How SBOMs can be operationalized by hospitals and healthcare organizations to improve procurement, asset visibility, and proactive risk management
Whether you are already generating SBOMs or just beginning your journey, you will leave with clear next steps and a stronger foundation for improving both compliance and real-world medical device security.
