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ISO SOP template

ISO SOP template

Achieve ISO compliance with this structured SOP template. It helps document processes and standards required for certification. Use this template to ensure quality management and regulatory adherence.

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ISO SOP template

Achieve ISO compliance with this structured SOP template. It helps document processes and standards required for certification. Use this template to ensure quality management and regulatory adherence.

Use this template with Lumiform

  • Customize this template or build your own
  • Fill out templates via mobile app
  • Get reports and analyse your data
Prices start from ░░░ per month
Book a demo
Learn more
or Download template as PDF

The ISO SOP template provides a standardized framework for documenting procedures that comply with ISO quality management requirements. Unlike generic process documents, this template specifically structures your SOPs to meet ISO standards with clearly defined sections for purpose, scope, responsibilities, and step-by-step instructions.

You’ll solve the common challenge of inconsistent documentation that fails audits—like when your team follows different formats across departments, causing compliance gaps. According to ISO 9001:2015, documented information must be controlled to ensure availability and protection from improper use, which this template helps you achieve through its structured approach to procedure documentation.

Related categories

  • Operational excellence templates
  • General templates
  • Templates for business processes
Preview of the template
Quality Management
Is the quality policy established, documented, implemented, and maintained?
Are responsibilities and authorities for quality-related roles defined?
Are procedures for management reviews established and maintained?
Are processes for internal audits established and maintained?
Documentation Practices
Are procedures for document and data control established and maintained?
Are records identified, stored, protected, retrieved, and disposed of?
Are procedures for control of quality records established and maintained?
Continuous Improvement
Are procedures for corrective and preventive action established and maintained?
Are processes for continual improvement of the quality management system established?
Are procedures for handling of customer complaints established and maintained?

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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.

Mastering standard operating procedure (SOP): A step-by-step guideISO 19600: A complete guide (with examples)ISO 17020: A deep dive into inspection body standardsISO 31000: Risk management for businesses
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Template collections

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Top 26 free SOP templates for every industry3 free ISO 31000 risk assessment templatesTop 6 free ISO 45001 audit checklist templatesBest 6 free ISO 27001 checklists for compliance
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Use cases

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SOP softwareISO softwareEquipment maintenance software Risk management software for anticipating and adressing safety risks
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Other resources

Explore all the additional resources we offer to assist you in mastering this topic.

10 clauses of ISO 90015 lean principles: The cycle of continuous improvementWhat is ISO 9001?4 benefits of safety management and how to communicate them

Frequently asked questions

What makes an ISO SOP template different from a regular procedure document?

An ISO SOP template is specifically structured to meet international standards requirements with mandatory sections like purpose, scope, and responsibilities. Regular procedure documents might lack this standardized approach, making them insufficient for compliance audits. ISO templates also include version control and approval mechanisms essential for quality management systems.

How do I customize the ISO SOP template for my specific industry needs?

Start by identifying your industry’s specific ISO requirements and regulatory obligations. Modify the template’s scope section to reflect your particular processes while keeping the core structure intact. Add industry-specific terminology and reference relevant standards or regulations that apply to your operations without altering the fundamental ISO-required sections.

Who should approve ISO SOPs before implementation?

ISO SOPs typically require approval from the process owner, quality manager, and department head responsible for the procedure. For critical processes, consider additional approval from senior management. This multi-level approval ensures technical accuracy, quality system alignment, and management commitment—all essential elements for effective implementation and ISO compliance.

How detailed should the procedure steps be in my ISO SOP?

Your procedure steps should be detailed enough for a qualified person to complete the task consistently without additional guidance. Focus on critical control points and decisions rather than obvious actions. Include enough detail to ensure compliance and consistency, but avoid over-specification that makes the document cumbersome to maintain and follow.


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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