On-Demand
Medical device cybersecurity expectations are becoming more stringent, with regulators such as the FDA and global frameworks like the IMDRF requiring greater transparency into software components and faster vulnerability response. Meeting these expectations depends on automated, repeatable SBOM workflows that produce high-fidelity, machine-readable SBOMs, continuously monitor components against vulnerability intelligence, and enable rapid triage and communication of risks.
In this webinar, you will learn key medical device cybersecurity requirements and practical methods for uncovering deeply embedded third-party components within firmware. You will identify gaps caused by incomplete SBOMs and improve how vulnerabilities are detected, prioritized, and communicated. The session also includes an SBOM management workflow that simplifies SBOM generation, validation, monitoring, and operational use, both for manufacturers and healthcare providers, with clear next steps to strengthen security and regulatory readiness.
This webinar is designed for medical device manufacturers, including product security, engineering, and compliance teams, as well as healthcare providers such as hospital IT, cybersecurity, and procurement professionals responsible for managing device risk. It is also relevant for anyone involved in SBOM generation, vulnerability management, or regulatory readiness in the medical device ecosystem.
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