Cybersecurity in Medical Devices¶
Food, U. S., Drug Administration, C. f. D., Health, R., Evaluation, C. f. B., & Research. Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions: Guidance for Industry and Food and Drug Administration Staff.
Cited by¶
1 citation across 1 artifact.
Each citation links to the sentence it supports in the citing article.
Mechanisms¶
- Software Bill of Materials with Lineage
- Regulators now expect a bill of materials for exactly this reason.
This sourceGuidance for Industry and FDA Staff. U.S. Food and Drug Administration (2023). Requires or recommends medical-device SBOMs that inventory third-party and upstream software dependencies for cybersecurity risk management.
- Regulators now expect a bill of materials for exactly this reason.
Verification¶
Does it exist? Not checked yet. This entry carries no identifier to resolve. It was extracted from the citation as written in the article, normalized, and deduplicated against the rest of the registry.
Does it back the claim? Not recorded. The single citation of this work carries no recorded support check.
Support is checked per citation rather than per work — the same source can be cited soundly in one article and wrongly in another. Per-citation recording began recently, so a citation with no recorded check is a gap in the record rather than evidence it went unchecked.
See how references were verified.
Registry ID ref:61840d13d136 · see in the full table