IEC 62304 Process Documents¶
The development of LQMS follows a process oriented on IEC 62304. This folder contains the process documents (plans and process descriptions). Records produced by executing these processes (reviews, test results, …) are tracked as described in the individual plans.
| Document | IEC 62304 reference |
|---|---|
| software_development_plan.md | 5.1 Software development planning |
| risk_management.md | 4.2 / 7 Risk management (with ISO 14971) |
| configuration_management_plan.md | 8 Software configuration management |
| problem_resolution.md | 9 Software problem resolution |
| verification_plan.md | 5.5–5.7 Unit/integration/system verification |
Note: LQMS itself is a tool supporting an ISO 13485 QMS, not a medical device. The IEC 62304-compliant process is a self-imposed quality measure; the safety classification and resulting process rigor are defined in the software development plan.
TBD: confirm safety classification rationale (expected: Class A equivalent / tool validation context per ISO 13485 §4.1.6).