medical-cybersecurity-report

仓库创建 2026年7月8日最近提交 3 天前SkillHot 收录 7 小时前

▸ 精选理由

帮助医疗器械团队快速产出合规草案并标注证据缺口。

▸ 风险提示

可能处理敏感医疗/合规数据，须严格脱敏与人工复核

这个 Skill 做什么

根据项目证据文件生成医疗器械网络安全注册与合规草案。

能把项目里的 DOCX/PDF/PNG 等证据文件读一遍，生成医疗器械网络安全的注册草案、风险分析、STRIDE 威胁模型、SBOM 注释和缺失信息清单。用在准备合规材料、整理项目事实或做内部风险评审时，把手头文档里的产品细节自动抽取出来并形成草稿。特别之处是会把没有证据支撑的结论标注为缺口，输出作为受控草稿，最后还需要人工复核和确认。

▸ 展开 SKILL.md 英文原文

Generate medical device cybersecurity registration deliverables from project input files. Use when Codex needs to read DOCX/PDF/PNG project evidence such as user manuals, SRS, design documents, architecture diagrams, FDA cybersecurity guidance, or prior reports, then produce a cybersecurity risk management report draft, project fact sheet, missing-information list, traceability content, STRIDE threat model, risk analysis, SBOM/security-transparency notes, or user-manual cybersecurity supplement.

垂直行业医疗网络安全合规模板证据驱动通用

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安装 / 使用

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帮我安装这个 skill：https://raw.githubusercontent.com/OpenAisec/Miko/main/data/skills/medical-cybersecurity-report/SKILL.md

或 curl 直取 SKILL.md

curl -fsSL "https://raw.githubusercontent.com/OpenAisec/Miko/main/data/skills/medical-cybersecurity-report/SKILL.md"

SKILL.MD 节选查看完整文件 ↗

# Medical Cybersecurity Report

Use this skill to produce high-completion cybersecurity registration drafts for medical device projects. Treat the output as a controlled draft: derive product-specific facts from evidence, mark unsupported claims as gaps, and require human review for final regulatory, quality, test, SBOM, and vulnerability conclusions.

Reusable scripts, references, and templates are stored in this skill folder. Project-specific generated deliverables are written only to the project output folder passed by `--output`.

## Required Workflow

1. Inventory the project folder. Identify input documents, output targets, prior reports, architecture images, and regulatory references.

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