{"id":6159,"date":"2026-08-22T08:47:58","date_gmt":"2026-08-22T12:47:58","guid":{"rendered":"https:\/\/www.isobudgets.com\/shop\/?post_type=product&p=6159"},"modified":"2026-09-09T00:18:59","modified_gmt":"2026-09-09T04:18:59","slug":"quality-manual-template","status":"publish","type":"product","link":"https:\/\/www.isobudgets.com\/shop\/product\/quality-manual-template\/","title":{"rendered":"ISOBudgets ISO\/IEC 17025:2017 Quality Manual Template (3rd Edition) | Audit-Ready System"},"content":{"rendered":"
\n

Get the ISO 17025 Quality Manual Template
\nand be audit-ready in 30 days or less.<\/strong><\/h2>\n

Want to get your laboratory ISO\/IEC 17025 accredited?<\/strong><\/p>\n

If so, you need a quality management system that meets the standard\u2019s requirements.<\/p>\n

Creating a system on your own can be time consuming. Most laboratories, that we speak with, spend 6 to 12 months making their own quality management system.<\/p>\n

Don’t spend 6 months creating a quality manual.<\/strong> Get the ISO 17025 Quality Manual Template and be audit-ready in 30 days or less.<\/p>\n

This is a complete quality management system for ISO\/IEC 17025:2017, including:<\/p>\n

    \n
  • 1 Quality Manual,<\/li>\n
  • 12 Procedures,<\/li>\n
  • 15 Lists,<\/li>\n
  • 21 Forms<\/li>\n
  • A file folder system (to store your documents and records), and<\/li>\n
  • An action plan checklist (to prepare for ISO\/IEC 17025 assessment).<\/li>\n<\/ul>\n

    The template gives you a management system that is 90% complete. You just need to review and update it to make it yours. Then, implement the policies and procedures in your lab so you can begin collecting data and records to prepare for ISO\/IEC assessment.<\/p>\n

    Just dedicate 1 hour a day<\/strong> to customizing your quality manual template to complete it in 30 days or less.<\/p>\n<\/div>\n

    <\/div><\/div>\n
    \n

    What’s Included With the<\/br>ISO 17025 Quality Manual Template<\/strong><\/h2>\n

    The template gives you everything you need to prepare for ISO\/IEC 17025 accreditation. Below, you will find complete breakdown of what is included with the template.<\/p>\n<\/div>\n

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    QUALITY MANUAL<\/h5>\n

    Here is a list of the included sections.<\/p>\n

      \n
    1. Section 2.0:<\/strong> Introduction – How to Use the Manual<\/span><\/li>\n
    2. Section 3.0:<\/strong> Terms and Definitions<\/span><\/li>\n
    3. Section 4.1:<\/strong> Impartiality<\/span><\/li>\n
    4. Section 4.1:<\/strong> Confidentiality<\/span><\/li>\n
    5. Section 5.0:<\/strong> Organization<\/span><\/li>\n
    6. Section 6.1:<\/strong> General Resources<\/span><\/li>\n
    7. Section 6.2:<\/strong> Personnel<\/span><\/li>\n
    8. Section 6.3:<\/strong> Facilities and Environmental Conditions<\/span><\/li>\n
    9. Section 6.4:<\/strong> Equipment<\/span><\/li>\n
    10. Section 6.5:<\/strong> Metrological Traceability<\/span><\/li>\n
    11. Section 6.6:<\/strong> Externally Provided Products and Services<\/span><\/li>\n
    12. Section 7.1:<\/strong> Contract Review<\/span><\/li>\n
    13. Section 7.2:<\/strong> Selection, Verification, and Validation of Methods<\/span><\/li>\n
    14. Section 7.3:<\/strong> Sampling<\/span><\/li>\n
    15. Section 7.4:<\/strong> Handling of Items<\/span><\/li>\n
    16. Section 7.5:<\/strong> Technical Records<\/span><\/li>\n
    17. Section 7.6:<\/strong> Evaluating Measurement Uncertainty<\/span><\/li>\n
    18. Section 7.7:<\/strong> Ensuring the Validity of Results<\/span><\/li>\n
    19. Section 7.8:<\/strong> Reporting the Results<\/span><\/li>\n
    20. Section 7.9:<\/strong> Complaints<\/span><\/li>\n
    21. Section 7.10:<\/strong> Nonconforming Work<\/span><\/li>\n
    22. Section 7.11:<\/strong> Information Management<\/span><\/li>\n
    23. Section 8.1:<\/strong> Management System<\/span><\/li>\n
    24. Section 8.2:<\/strong> Management System Documentation<\/span><\/li>\n
    25. Section 8.3:<\/strong> Document Control<\/span><\/li>\n
    26. Section 8.4:<\/strong> Record Control<\/span><\/li>\n
    27. Section 8.5:<\/strong> Risks and Opportunities<\/span><\/li>\n
    28. Section 8.6:<\/strong> Improvement<\/span><\/li>\n
    29. Section 8.7:<\/strong> Corrective Actions<\/span><\/li>\n
    30. Section 8.8:<\/strong> Internal Audits<\/span><\/li>\n
    31. Section 8.9:<\/strong> Management Reviews<\/span><\/li>\n<\/ol>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t
      \n\t\t\t\t
      \n\t\t\t\n\t\t\t\n
      Procedures<\/h5>\n

      Here is a list of the included procedures.<\/p>\n

        \n
      1. SOP 01:<\/strong> Managing Personnel<\/span><\/li>\n
      2. SOP 02:<\/strong> Managing Laboratory Equipment<\/span><\/li>\n
      3. SOP 03:<\/strong> Intermediate Checks<\/span><\/li>\n
      4. SOP 04:<\/strong> Managing Products and Services<\/span><\/li>\n
      5. SOP 05:<\/strong> Reviewing Requests<\/span><\/li>\n
      6. SOP 06:<\/strong> Verifying & Validating Methods<\/span><\/li>\n
      7. SOP 07:<\/strong> Handling Items<\/span><\/li>\n
      8. SOP 08:<\/strong> Ensuring Validity of Results<\/span><\/li>\n
      9. SOP 09:<\/strong> Handling Complaints<\/span><\/li>\n
      10. SOP 10:<\/strong> Handling Nonconforming Work<\/span><\/li>\n
      11. SOP 11:<\/strong> Conducting Internal Audits<\/span><\/li>\n<\/ol>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t
        \n\t\t\t\t
        \n\t\t\t\n\t\t\t\n
        LISTS<\/h5>\n

        Here is a list of the included lists and logs.<\/p>\n

          \n
        1. List 01:<\/strong> Master Document List<\/span><\/li>\n
        2. List 02:<\/strong> Distribution List<\/span><\/li>\n
        3. List 03:<\/strong> Qualification List<\/span><\/li>\n
        4. List 04:<\/strong> Laboratory Training Log<\/span><\/li>\n
        5. List 05:<\/strong> Equipment Maintenance List<\/span><\/li>\n
        6. List 06:<\/strong> Reference Values and Correction Factors<\/span><\/li>\n
        7. List 07:<\/strong> Supplier List<\/span><\/li>\n
        8. List 08:<\/strong> Purchase Log (Supplies and Services)<\/span><\/li>\n
        9. List 09:<\/strong> Method List<\/span><\/li>\n
        10. List 10:<\/strong> Multi-Year PT\/ILC Plan (with Risk)<\/span><\/li>\n
        11. List 11:<\/strong> Feedback Log<\/span><\/li>\n
        12. List 12:<\/strong> Nonconforming Work Log<\/span><\/li>\n
        13. List 13:<\/strong> LIMS Management Log<\/span><\/li>\n
        14. List 14:<\/strong> Risks and Opportunities List<\/span><\/li>\n
        15. List 15:<\/strong> Laboratory Temperature Log (\u00b0C)<\/span><\/li>\n
        16. List 16:<\/strong> Laboratory Temperature Log (\u00b0F)<\/span><\/li>\n
        17. List 17:<\/strong> Laboratory Temperature & Humidity Log (\u00b0C)<\/span><\/li>\n
        18. List 18:<\/strong> Laboratory Temperature & Humidity Log (\u00b0F)<\/span><\/li>\n<\/ol>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t
          \n\t\t\t\t
          \n\t\t\t\n\t\t\t\n
          FORMS<\/h5>\n

          Here is a list of the included forms and documents.<\/p>\n

            \n
          1. Form 01:<\/strong> Impartiality Agreement<\/span><\/li>\n
          2. Form 02:<\/strong> Confidentiality Agreement<\/span><\/li>\n
          3. Form 03:<\/strong> Read and Understand Log<\/span><\/li>\n
          4. Form 04:<\/strong> Competence Requirements Worksheet<\/span><\/li>\n
          5. Form 05:<\/strong> Monitoring Personnel Competence Form<\/span><\/li>\n
          6. Form 06:<\/strong> Equipment Check-In\/Check-Out Log<\/span><\/li>\n
          7. Form 07:<\/strong> Intermediate Check Form<\/span><\/li>\n
          8. Form 08:<\/strong> Purchase Request Form<\/span><\/li>\n
          9. Form 09:<\/strong> Product\/Service Inspection Form<\/span><\/li>\n
          10. Form 10:<\/strong> Service Request Form<\/span><\/li>\n
          11. Form 11:<\/strong> Contract Review Form<\/span><\/li>\n
          12. Form 12:<\/strong> Method Development Form<\/span><\/li>\n
          13. Form 13:<\/strong> Method Verification Form<\/span><\/li>\n
          14. Form 14:<\/strong> Method Validation Form<\/span><\/li>\n
          15. Form 15:<\/strong> Public Complaint Handling Process<\/span><\/li>\n
          16. Form 16:<\/strong> Corrective Action Form<\/span><\/li>\n
          17. Form 17:<\/strong> Internal Audit Plan<\/span><\/li>\n
          18. Form 18:<\/strong> Internal Audit Checklist<\/span><\/li>\n
          19. Form 19:<\/strong> Laboratory Witnessing Form<\/span><\/li>\n
          20. Form 20:<\/strong> Laboratory Tracing Form<\/span><\/li>\n
          21. Form 21:<\/strong> Assessment Finding Form<\/span><\/li>\n
          22. Form 22:<\/strong> Scope Audit Form<\/span><\/li>\n
          23. Form 23:<\/strong> PT Participation Audit Form<\/span><\/li>\n
          24. Form 24:<\/strong> Management Review Form<\/span><\/li>\n
          25. Form 25:<\/strong> Organization Chart<\/span><\/li>\n<\/ol>\n\t\t<\/div>\n\t\t\t\t\n