FDA SBOM requirements under Section 524B for medical devi...
What Section 524B means for medical device makers: FDA SBOM requirements, premarket cybersecurity guidance, and how to avoid a Refuse to Accept letter.
Deep dives, practical guides, and incident analyses from engineers who build Safeguard. No fluff, no vendor FUD — just what you need to ship secure software.
What Section 524B means for medical device makers: FDA SBOM requirements, premarket cybersecurity guidance, and how to avoid a Refuse to Accept letter.
CVE-2023-26136: a prototype pollution flaw in tough-cookie hides deep in transitive Node.js dependencies. Impact, timeline, and remediation steps.
HIPAA doesn't name software composition analysis, but auditors increasingly expect it. Here's how healthcare teams use SCA to manage third-party risk and protect ePHI.
How the Change Healthcare breach, weak EHR vendor risk management, and exposed HL7 FHIR APIs turned healthcare's software supply chain into its biggest security gap.
How medical device firmware SBOMs, FDA Section 524B, ISO 81001-5-1, and coordinated vulnerability disclosure work together to secure connected IoMT devices.
CVE-2024-21538 is a ReDoS flaw in the widely-used cross-spawn npm package. Learn the impact, CVSS/EPSS context, and how to remediate it.
CVE-2024-29041 lets attackers weaponize Express.js redirects for phishing. See affected versions, CVSS/EPSS data, and how to remediate fast.
A six-step playbook for telehealth vendor risk management: inventory PHI flows, tier HIPAA business associate risk, run SCA on vendor SDKs, and monitor continuously.
CVE-2022-25881 lets attacker-influenced HTTP responses trigger catastrophic regex backtracking in http-cache-semantics, hanging Node.js services. Here's how to detect and fix it.
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