Creates reference documentation structure (docs/reference/ with README, adrs/, guides/, manuals/ directories). Second worker in ln-110-documents-pipeline.
WHAT YOU BECOME
Perfect for these scenarios
Ensure full compliance with ISO 14971 throughout product lifecycle
Conduct thorough risk analyses and evaluations for medical devices
Verify effectiveness of implemented risk control measures
Analyze post-production data to update risk management files
MEASURED GAIN
Proven benefits and measurable impact
Speed up approval processes with well-documented risk files
Reduce time spent on risk assessments by automating documentation
Minimize recalls by proactively identifying and mitigating risks
WHAT YOU GET
Files, tags and the three-step install
Tip: Read the documentation and the code before first use, so you know what it does and which permissions it needs.
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