Control ISO 9001 Risks and CAPAs - With Auditor-Ready Documentation

A structured ISO 9001 risk and corrective action system aligned to Clause 6.1 and Clause 10 - including risk register, CAPA log, root cause analysis, and action tracking templates used by ISO consultants and compliance teams.
What ISO consultants charge $300–$1,000 for, you get instantly for $39
Download The ISO 9001 Risk & CAPA Pack
One-time purchase · Instant download · $39

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.

WHAT THIS IS

This is not a single risk register.

This is a complete ISO 9001 Risk & CAPA system.

It includes every document an ISO auditor expects to see for risk-based thinking and corrective action - from risk identification and evaluation through root cause analysis, corrective action tracking, and effectiveness verification.

THIS PACK ALLOWS YOU TO:

  • 1
    Demonstrate structured risk-based thinking
  • 2
    Document identified risks and opportunities
  • 3
    Perform root cause analysis for non-conformities
  • 4
    Track corrective actions to closure
  • 5
    Verify effectiveness and retain audit evidence

Included In The Risk & CAPA Pack

8 professionally structured registers and trackers. Audit-ready, practical, and fully editable.

  • Risk Register

    Central log of identified risks, risk owners, impact, likelihood, and current status.

  • Risk Assessment Matrix

    Defines risk scoring methodology using likelihood and impact evaluation criteria.

  • Risk Treatment Plan

    Documents selected risk treatment options, actions, responsibilities, and timelines.

  • Non-Conformance Log

    Records identified non-conformities, sources, clause references, and status tracking.

  • Root Cause Analysis

    Structured analysis to identify underlying causes of non-conformities and incidents.

  • Corrective Action Register

    Tracks corrective actions, responsible owners, target dates, and completion status.

  • Preventive Action Plan

    Identifies proactive actions to prevent recurrence of potential non-conformities.

  • 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 Register

Risk Assessment Matrix

Risk Assessment Matrix

Risk Treatment Plan

Risk Treatment Plan

Non-Conformance Register

Non-Conformance Register

Root Cause Analysis

Root Cause Analysis

Corrective Action Register

Corrective Action Register

Corrective And Preventive Action Plan

Corrective And Preventive Action Plan

Calibration Equipment Tracker

Calibration Equipment Tracker
ISO 9001 Risk & CAPA Toolkit

Get Risk-Controlled Today

Download the complete ISO 9001 Risk & CAPA Pack - practical, audit-ready documents to identify risks, manage nonconformities, and implement effective corrective actions.
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Lifetime Access
Use Across Unlimited Risk & Corrective Action Cycles
Suitable For ISO 9001 Risk-Based Thinking and CAPA Implementation
$39
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All-In-One Consultant Package

For consultants managing multiple clients. Includes ISO 9001, ISO 27001, ISO 20000, IT Governance, audit frameworks, and full client delivery systems.
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