Control ISO 9001 Risks and CAPAs - With Auditor-Ready Documentation
Who This Is For
Quality Managers
Running internal audits as part of your QMS maintenance and improvement cycle.
ISO Consultants
Managing client audits and delivering professional audit documentation.
Organizations
Preparing for certification or surveillance audits.
This is not a single risk register.
This is a complete ISO 9001 Risk & CAPA system.
THIS PACK ALLOWS YOU TO:
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1Demonstrate structured risk-based thinking
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2Document identified risks and opportunities
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3Perform root cause analysis for non-conformities
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4Track corrective actions to closure
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5Verify effectiveness and retain audit evidence
Included In The Risk & CAPA Pack
8 professionally structured registers and trackers. Audit-ready, practical, and fully editable.
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Risk Register
Central log of identified risks, risk owners, impact, likelihood, and current status.
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Risk Assessment Matrix
Defines risk scoring methodology using likelihood and impact evaluation criteria.
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Risk Treatment Plan
Documents selected risk treatment options, actions, responsibilities, and timelines.
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Non-Conformance Log
Records identified non-conformities, sources, clause references, and status tracking.
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Root Cause Analysis
Structured analysis to identify underlying causes of non-conformities and incidents.
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Corrective Action Register
Tracks corrective actions, responsible owners, target dates, and completion status.
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Preventive Action Plan
Identifies proactive actions to prevent recurrence of potential non-conformities.
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Calibration Equipment Tracker
Ensures corrective and preventive actions are implemented and deliver intended outcomes.
See The Exact Risk & CAPA Documents You Receive
These are the same documents used to manage risk and corrective actions.
Risk Register
Risk Assessment Matrix
Risk Treatment Plan
Non-Conformance Register
Root Cause Analysis
Corrective Action Register
Corrective And Preventive Action Plan
Calibration Equipment Tracker
Get Risk-Controlled Today
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