An internal audit of your medical device quality management system is essential for ISO 13485 compliance. This skill helps you plan and run audits step by step. You can classify findings and verify corrective actions with confidence.
Use it to create an audit schedule based on risk. Assign independent auditors and check each QMS clause. The skill also guides you through collecting evidence and writing reports.
Whether you are preparing for an external audit or managing an ongoing audit program, this tool makes the process clear and repeatable. It works for any medical device company that follows ISO 13485.
Global
mkdir -p ~/.claude/skills/qms-audit-expertProject
mkdir -p .claude/skills/qms-audit-expertSource Repository
Healthcare Emr Patternsaffaan-m/everything-claude-code
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Healthcare Cdss Patternsaffaan-m/everything-claude-code
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Mfds Food Safetynomadamas/k-skill
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Mfds Drug Safetynomadamas/k-skill
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Healthkitdpearson2699/swift-ios-skills
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Sensorkitdpearson2699/swift-ios-skills
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Ggetaffaan-m/everything-claude-code
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Single Cell Rna Qcanthropics/knowledge-work-plugins
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