iso-standards-compliance-checker
Medical device standards compliance verification skill for ISO 13485, ISO 14971, IEC 62304, IEC 60601, and related standards
Best use case
iso-standards-compliance-checker is best used when you need a repeatable AI agent workflow instead of a one-off prompt.
Medical device standards compliance verification skill for ISO 13485, ISO 14971, IEC 62304, IEC 60601, and related standards
Teams using iso-standards-compliance-checker 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/iso-standards-compliance-checker/SKILL.mdinside your project - Restart your AI agent — it will auto-discover the skill
How iso-standards-compliance-checker Compares
| Feature / Agent | iso-standards-compliance-checker | 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 standards compliance verification skill for ISO 13485, ISO 14971, IEC 62304, IEC 60601, and related standards
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
# ISO Standards Compliance Checker Skill
## Purpose
The ISO Standards Compliance Checker Skill verifies medical device compliance with applicable ISO and IEC standards, generating compliance checklists, gap analyses, and evidence mapping for quality management and regulatory submissions.
## Capabilities
- Standards applicability determination
- Compliance checklist generation
- Gap analysis against standard clauses
- Evidence mapping to requirements
- Harmonized standards cross-reference
- Declaration of Conformity assistance
- Audit preparation support
- Non-conformance tracking
- Corrective action recommendations
- Standards version comparison
- Multi-standard compliance matrices
## Usage Guidelines
### When to Use
- Implementing quality management systems
- Preparing for certification audits
- Conducting internal compliance reviews
- Supporting regulatory submissions
### Prerequisites
- Device type and intended use defined
- Applicable regulatory pathways identified
- Quality management system documentation available
- Design and development records accessible
### Best Practices
- Identify all applicable standards early in development
- Maintain current knowledge of standards revisions
- Document compliance evidence systematically
- Conduct regular internal compliance reviews
## Process Integration
This skill integrates with the following processes:
- Design Control Process Implementation
- Medical Device Risk Management (ISO 14971)
- Software Development Lifecycle (IEC 62304)
- EU MDR Technical Documentation
## Dependencies
- ISO standards database
- FDA recognized consensus standards list
- Harmonized standards registry
- Standards development organization publications
- Regulatory guidance documents
## Configuration
```yaml
iso-standards-compliance-checker:
standards-families:
- ISO-13485
- ISO-14971
- IEC-62304
- IEC-60601
- ISO-10993
- ISO-11135
- ISO-11137
- ISO-11607
compliance-levels:
- full
- partial
- not-applicable
output-formats:
- checklist
- gap-analysis
- evidence-matrix
```
## Output Artifacts
- Standards applicability matrices
- Compliance checklists by standard
- Gap analysis reports
- Evidence mapping documents
- Declaration of Conformity templates
- Audit preparation packages
- Non-conformance logs
- Corrective action recommendations
## Quality Criteria
- All applicable standards identified correctly
- Checklists reflect current standard versions
- Gap analysis is comprehensive and actionable
- Evidence mapping supports audit review
- Documentation maintains regulatory acceptance
- Compliance status accurately reportedRelated Skills
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