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ISO 9001 supplier audit checklist template

ISO 9001 supplier audit checklist template

Assess suppliers’ quality management systems against ISO 9001 requirements to ensure compliance and identify improvement opportunities.

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The Lumiform application helps frontline teams uphold internal standards effortlessly.
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ISO 9001 supplier audit checklist template

Assess suppliers’ quality management systems against ISO 9001 requirements to ensure compliance and identify improvement opportunities.

Use this template with Lumiform

The Lumiform application helps frontline teams uphold internal standards effortlessly.
  • Customize this template or build your own
  • Fill out templates via mobile app
  • Assign and track corrective actions
  • Get reports and analyse your data
Prices start from ░░░ per month
Book a demo
Learn more
or Download template as PDF

The ISO 9001 supplier audit checklist provides a framework for evaluating current and prospective suppliers against critical quality management system requirements. It allows you to address key ISO 9001 components, from quality management system documentation to measurement and improvement processes.

Research from the Business Continuity Institute reveals that 72% of organizations have faced at least one supply chain disruption, with most experiencing multiple disruptions. This template serves as your initial line of defense by ensuring suppliers meet your quality standards. You can use this template during initial supplier selection to compare candidates objectively or for periodic audits of existing suppliers to maintain ongoing quality assurance and drive continuous improvement.

Related categories

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Preview of the template
Page 1
Supplier Information
Supplier Name
Supplier Address
Auditor Name
Audit Date
Quality Management System
Does the supplier have a documented quality management system?
Does the supplier's quality management system meet the requirements of ISO 9001?
Are quality objectives established and reviewed?
Are all required procedures and records maintained?
Management Responsibility
Is top management commitment to the quality management system evident?
Are responsibilities and authorities defined and communicated?
Are management reviews conducted periodically?
Resource Management
Are adequate resources available to implement and maintain the quality management system?
Is the infrastructure suitable to achieve conformity to product requirements?
Are personnel competent based on education, training, skills and experience?
Product Realization
Are product requirements determined and reviewed?
Is the product design and development process established and implemented?
Is the purchasing process, including evaluation of subcontractors, defined and implemented?
Is production and service provision planned and carried out under controlled conditions?
Is monitoring and measurement of the product carried out at appropriate stages?
Measurement, Analysis and Improvement
Are processes for monitoring, measurement, analysis and improvement established?
Is internal auditing conducted periodically?
Is corrective and preventive action taken to address nonconformities?

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Related resources

Access a complete set of resources aimed at maximizing safety, quality, and operational excellence, including detailed guides, related templates, and real-world use cases.

Topic guides

Read in-depth guides covering key topics related to this article.

ISO 9001: An essential blueprint for creating quality products & servicesMastering supplier quality management: A comprehensive guideSupplier selection process: A complete guide
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ISO 9001 softwareSupplier quality management softwareSupplier audit softwareSupplier evaluation software
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10 clauses of ISO 9001Quality management processHow to evaluate compliance measuresHow to implement operational excellence

Frequently asked questions

How can you prepare suppliers for an audit using this checklist?

Share the audit checklist with suppliers well in advance, explaining its purpose is improvement rather than punishment. Clearly communicate your expectations and the ISO 9001 requirements they need to meet. Offer a pre-audit call to answer questions and address concerns. Give suppliers adequate time to gather necessary documentation and prepare their teams. This transparent approach helps reduce anxiety and creates a collaborative environment focused on quality improvement.

What documentation should suppliers have ready during an ISO 9001 audit?

Suppliers should prepare their quality manual, process documentation, and quality policy statements. They’ll need records of management reviews, internal audits, and corrective actions. Have training records and competency evaluations available for personnel. Calibration records for equipment, product-specific documentation, and evidence of continuous improvement activities are also essential.

How do you handle non-conformities identified during a supplier audit?

When you identify non-conformities, document them clearly with objective evidence. Categorize issues by severity (minor, major, critical) and communicate findings professionally during the closing meeting. Request a corrective action plan with root cause analysis and implementation timelines. Follow up to verify effective implementation of corrective actions. For serious issues, consider additional verification through a follow-up audit.

Can you customize this ISO 9001 supplier audit checklist for your specific industry?

Yes, Lumiform makes it convenient. First, review the standard checklist and identify sections needing industry-specific requirements. Add questions addressing unique regulatory requirements for your industry. You can also Incorporate relevant industry standards and best practices beyond basic ISO 9001 requirements. Test the customized checklist with a pilot audit and refine based on feedback before full implementation.


This template, developed by Lumiform employees, serves as a starting point for businesses using the Lumiform platform and is intended as a hypothetical example only. It does not replace professional advice. Companies should consult qualified professionals to assess the suitability and legality of using this template in their specific workplace or jurisdiction. Lumiform is not liable for any errors or omissions in this template or for any actions taken based on its content.
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