ISO 13485 Medical Device QMS Starter
Quality manual, 10 core procedures, DHF/DMR/DHR templates, ISO 14971-style risk file, CAPA and complaint logs.
What's inside →Home / Medical / Medical Device Software Kit (IEC 62304)

Lifecycle checklist, requirements-to-test traceability, SOUP register, problem reports, SDP and release checklist. Templates, not regulatory advice.
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Small medical device makers, startups and contract manufacturers building or tightening an ISO 13485 / FDA quality system.
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Quality manual, 10 core procedures, DHF/DMR/DHR templates, ISO 14971-style risk file, CAPA and complaint logs.
What's inside →Gap assessment mapping the old QSR to the QMSR / ISO 13485, a records matrix and a transition plan. Templates, not regulatory advice.
What's inside →Risk plan, hazard analysis tied to an editable acceptability matrix, FMEA, benefit-risk and the risk management report. Templates, not regulatory advice.
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