Management Review Preparation Checklist [FREE PDF]

Management reviews are a mandatory requirement under ISO 9001:2015 Clause 9.3, requiring top management to evaluate the suitability, adequacy, and effectiveness of the quality management system at planned intervals. Organizations must compile and present specific input data including audit results, customer feedback, process performance, and nonconformity trends before conducting the review. This checklist ensures all required inputs are gathered, reviewed, and documented to support evidence-bas

  • Industry: Quality Assurance
  • Frequency: Quarterly
  • Estimated Time: 60-90 minutes
  • Role: QA Manager
  • Total Items: 33
  • Compliance: ISO 9001:2015 Clause 9.3 - Management Review, AS9100 Rev D Clause 9.3.2 - Management Review Inputs, IATF 16949:2016 Clause 9.3.1 - Management Review General, ISO 13485:2016 Clause 5.6 - Management Review, ISO 9001:2015 Clause 10.2 - Nonconformity and Corrective Action

Follow-Up from Previous Management Review

Verify all action items from the prior management review have been addressed and closed.

  • Have all action items from the previous management review been reviewed for status?
  • Are all overdue action items documented with a revised completion date and owner?
  • Has a summary of closed action items been prepared for presentation?
  • Have any recurring action items been escalated to risk management review?

Internal and External Audit Results

Compile and verify audit findings, trends, and corrective action status for management review input.

  • Have internal audit results from the review period been compiled and summarized?
  • Have external audit findings (e.g., registrar, customer) been included in the summary?
  • Is the trend of major vs. minor nonconformities across audits documented?
  • Are all open corrective actions from audits listed with current status?
  • Has the audit schedule effectiveness been evaluated for the period?

Customer Feedback and Satisfaction Data

Review customer satisfaction metrics, complaints, and VOC data for management presentation.

  • Has customer satisfaction data been collected and trend-analyzed for the period?
  • Have all formal customer complaints received during the period been summarized?
  • Are customer scorecards or supplier performance ratings from customers included?
  • Have any customer-specific requirements or regulatory changes been identified?
  • Is a written summary of VOC (Voice of Customer) themes prepared for leadership?

Process Performance and Product Conformity

Validate that KPIs, OEE, first-pass yield, and conformity data are compiled and current.

  • Have process performance KPIs for all key processes been compiled for the period?
  • Is first-pass yield or right-first-time (RFT) data available and trended?
  • Has scrap and rework cost data been quantified and presented in financial terms?
  • Are on-time delivery (OTD) metrics compiled and compared to targets?
  • Have significant process deviations or special cause variations been identified and documented?

Corrective and Preventive Action (CAPA) Status

Ensure all open CAPAs are summarized with effectiveness evaluations for management review.

  • Has a complete list of open CAPAs with owners and due dates been prepared?
  • Have effectiveness verifications for closed CAPAs been completed and documented?
  • Is the trend of CAPA cycle time (open to close) being tracked and improving?
  • Are recurrence rates for previously closed CAPAs monitored and reported?

Risks, Opportunities, and Strategic Changes

Review risk register updates, emerging opportunities, and any changes affecting the QMS.

  • Has the organizational risk register been updated and reviewed prior to this meeting?
  • Have changes in internal or external context (e.g., regulatory, market) been identified?
  • Are new business opportunities or product/service expansion initiatives documented for review?
  • Have supply chain risks identified during the period been escalated for management awareness?
  • Are resource adequacy concerns (personnel, equipment, infrastructure) identified for discussion?

Management Review Outputs and Documentation Readiness

Confirm all required outputs are planned and that meeting documentation is ready for capture.

  • Is a meeting agenda prepared and distributed to all required participants in advance?
  • Is a minutes/action item template ready to capture decisions and resource allocations?
  • Are continual improvement opportunities (process and product/service) identified for agenda?
  • Are quality objectives reviewed for achievement and proposed updates ready for discussion?
  • Has the previous management review record been archived and is accessible for reference?

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Why Use This Management Review Preparation Checklist [FREE PDF]?

This management review preparation checklist [free pdf] helps quality assurance teams maintain compliance and operational excellence. Designed for qa manager professionals, this checklist covers 33 critical inspection points across 7 sections. Recommended frequency: quarterly.

Ensures compliance with ISO 9001:2015 Clause 9.3 - Management Review, AS9100 Rev D Clause 9.3.2 - Management Review Inputs, IATF 16949:2016 Clause 9.3.1 - Management Review General, ISO 13485:2016 Clause 5.6 - Management Review, ISO 9001:2015 Clause 10.2 - Nonconformity and Corrective Action. Regulatory-aligned for audit readiness and inspection documentation.

Frequently Asked Questions

What does the Management Review Preparation Checklist [FREE PDF] cover?

This checklist covers 33 inspection items across 7 sections: Follow-Up from Previous Management Review, Internal and External Audit Results, Customer Feedback and Satisfaction Data, Process Performance and Product Conformity, Corrective and Preventive Action (CAPA) Status, Risks, Opportunities, and Strategic Changes, Management Review Outputs and Documentation Readiness. It is designed for quality assurance operations and compliance.

How often should this checklist be completed?

This checklist should be completed quarterly. Each completion takes approximately 60-90 minutes.

Who should use this Management Review Preparation Checklist [FREE PDF]?

This checklist is designed for QA Manager professionals in the quality assurance industry. It can be used for self-assessments, team audits, and regulatory compliance documentation.

Can I download this checklist as a PDF?

Yes, this checklist is available as a free PDF download. You can also use it digitally in the POPProbe mobile app for real-time data capture, photo documentation, and automatic reporting.

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