iec-62304
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npx mdskill add mkurman/zorai/iec-62304Classify medical device software safety and manage regulatory compliance.
- Assigns Class A/B/C risk levels and generates FDA/EU MDR documentation.
- Integrates ISO 14971 risk management and cybersecurity threat modeling.
- Executes design control workflows from requirements through verification.
- Outputs structured reports for software development plans and test results.
SKILL.md
.github/skills/iec-62304View on GitHub ↗
--- name: iec-62304 description: "IEC 62304 medical device software lifecycle framework. Risk classification, software safety classification (A/B/C), design control, verification, validation, and regulatory documentation for FDA/EU MDR submissions." tags: [iec-62304, medical-device, regulatory, compliance, fda, safety, zorai] --- ## Overview IEC 62304 medical device software lifecycle framework. Software safety classification (Class A/B/C), design control, verification, validation, and regulatory documentation for FDA and EU MDR submissions. ## Software Safety Classification - **Class A** -- No injury or damage to health (e.g., log viewer) - **Class B** -- Non-serious injury (e.g., infusion pump alarm) - **Class C** -- Death or serious injury (e.g., radiation therapy planning) ## Key Processes - **Design Control** -- Requirements -> Design -> Implementation -> Verification -> Validation - **Risk Management (ISO 14971)** -- Hazard identification, risk estimation, risk control - **Software Change Management** -- Change classification (bug fix, enhancement, new feature) - **Problem Resolution** -- CAPA for software defects - **Cybersecurity** -- Threat modeling, vulnerability management ## Documentation Checklist ``` - Software Development Plan - Software Requirements Specification - Software Architecture Document - Software Detailed Design - Software Unit Verification - Software Integration Testing - Software System Testing - Software Release Notes - Software Maintenance Plan - Software Risk Management File ```