iec62304-lifecycle-manager
Medical device software lifecycle management skill implementing IEC 62304 requirements
Best use case
iec62304-lifecycle-manager is best used when you need a repeatable AI agent workflow instead of a one-off prompt.
Medical device software lifecycle management skill implementing IEC 62304 requirements
Teams using iec62304-lifecycle-manager should expect a more consistent output, faster repeated execution, less prompt rewriting.
When to use this skill
- You want a reusable workflow that can be run more than once with consistent structure.
When not to use this skill
- You only need a quick one-off answer and do not need a reusable workflow.
- You cannot install or maintain the underlying files, dependencies, or repository context.
Installation
Claude Code / Cursor / Codex
Manual Installation
- Download SKILL.md from GitHub
- Place it in
.claude/skills/iec62304-lifecycle-manager/SKILL.mdinside your project - Restart your AI agent — it will auto-discover the skill
How iec62304-lifecycle-manager Compares
| Feature / Agent | iec62304-lifecycle-manager | Standard Approach |
|---|---|---|
| Platform Support | Not specified | Limited / Varies |
| Context Awareness | High | Baseline |
| Installation Complexity | Unknown | N/A |
Frequently Asked Questions
What does this skill do?
Medical device software lifecycle management skill implementing IEC 62304 requirements
Where can I find the source code?
You can find the source code on GitHub using the link provided at the top of the page.
SKILL.md Source
# IEC 62304 Lifecycle Manager Skill
## Purpose
The IEC 62304 Lifecycle Manager Skill supports medical device software lifecycle management per IEC 62304, ensuring proper classification, documentation, and maintenance of software as a medical device (SaMD) and software in medical devices (SiMD).
## Capabilities
- Software safety classification (Class A, B, C)
- Software development plan template generation
- SOUP (Software of Unknown Provenance) management
- Software architecture documentation templates
- Anomaly and problem tracking
- Configuration management guidance
- Maintenance planning
- Software requirements specification templates
- Unit/integration test planning
- Release documentation
- Change control workflows
## Usage Guidelines
### When to Use
- Planning medical device software projects
- Classifying software safety levels
- Managing SOUP components
- Preparing for regulatory submissions
### Prerequisites
- Device intended use defined
- Software scope identified
- Hazard analysis completed
- Development team resources available
### Best Practices
- Classify software based on hazard analysis
- Document all SOUP with risk assessments
- Maintain comprehensive change control
- Plan maintenance activities from project start
## Process Integration
This skill integrates with the following processes:
- Software Development Lifecycle (IEC 62304)
- Software Verification and Validation
- AI/ML Medical Device Development
- Medical Device Risk Management (ISO 14971)
## Dependencies
- IEC 62304 standard
- AAMI TIR45 guidance
- Configuration management tools
- Issue tracking systems
- Development environments
## Configuration
```yaml
iec62304-lifecycle-manager:
safety-classes:
- Class-A
- Class-B
- Class-C
lifecycle-phases:
- planning
- requirements
- architecture
- detailed-design
- implementation
- verification
- release
- maintenance
document-types:
- development-plan
- requirements-spec
- architecture-doc
- test-plans
- release-notes
```
## Output Artifacts
- Software development plans
- Safety classification rationale
- SOUP management documentation
- Architecture documents
- Requirements specifications
- Anomaly management reports
- Configuration management plans
- Maintenance plans
## Quality Criteria
- Safety classification justified by hazard analysis
- Documentation appropriate for safety class
- SOUP properly evaluated and controlled
- Configuration management comprehensive
- Anomaly management effective
- Maintenance activities plannedRelated Skills
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