THE PERFECT ISO 17025 QUALITY MANUAL TEMPLATE FOR BUSY LABS

  • Don’t Spend 6 Months Creating a Quality Manual. Get Ready for ISO 17025 Accreditation in 30 Days or Less with this Complete Quality Manual Template

    Includes:

    • 1 Quality Manual
    • 12 Procedures
    • 14 Lists
    • 18 Forms

    Buy the Quality Manual Template Now

  • ISO 17025 Quality Manual Template

 

“CREATE A CUSTOM ISO 17025 QUALITY MANUAL IN LESS THAN 30 DAYS”

(Just dedicate 1 hour a day to customizing your manual, procedures, forms, and lists)

 

  • Fill in the Blanks ISO 17025 Quality Manual Template

    Easy to Customize

    Just fill in the blanks to customize your quality manual. Plus, get expert tips included in the template.
  • Color Coded References ISO 17025 Quality Manual Template

    User Friendly

    Find information fast with color-coded text, bold headers, different font sizes, and lists.
  • Works for Most Labs

    Compatible with most types of laboratories: calibration, testing, chemical, & microbiology laboratories.

 
 

EVERYTHING YOU NEED FOR ISO/IEC 17025:2017 ACCREDITATION

THE ISO 17025 QUALITY MANUAL TEMPLATE INCLUDES…

 

  • ISO 17025 Quality Manual

    1 Quality Manual

  • ISO 17025 Procedures

    12 Procedures

  • ISO 17025 Lists and Logs

    14 Lists and Logs

  • ISO 17025 Forms

    18 Forms

 

See the Full List

 

  • Quality Manual

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

    1. SOP 01: Managing Personnel
    2. SOP 02: Managing Laboratory Equipment
    3. SOP 03: Intermediate Checks
    4. SOP 04: Purchasing Products and Services
    5. SOP 05: Reviewing Contracts
    6. SOP 06: Validating Methods
    7. SOP 07: Handling Items
    8. SOP 08: Ensuring Validity of Results
    9. SOP 09: Handling Complaints
    10. SOP 10: Handling Nonconforming Work
    11. SOP 11: Conducting Internal Audits
    12. SOP 12: Evaluating Measurement Uncertainty

     

    Lists

    1. List 01: Organization Chart
    2. List 02: Master Document List
    3. List 03: Distribution List
    4. List 04: Equipment List
    5. List 05: Training Log
    6. List 06: Qualification List
    7. List 07: Supplier List
    8. List 08: Purchase Log
    9. List 09: Method Validation Log
    10. List 10: PT/ILC Plan
    11. List 11: Complaint Log
    12. List 12: LIMS Log
    13. List 13: LIMS Error Log
    14. List 14: Risks and Opportunities List
  • Forms

    1. Form 01: Impartiality Agreement
    2. Form 02: Confidentiality Agreement
    3. Form 03: Competence Requirements Worksheet
    4. Form 04: Employee Training Log
    5. Form 05: Employee Evaluation Form
    6. Form 06: Purchase Order
    7. Form 07: Product/Service Inspection Form
    8. Form 08: CMethod Validation Form
    9. Form 09: Complaint Form
    10. Form 10: Handling Complaints Handout
    11. Form 11: Nonconformance Form
    12. Form 12: Customer Survey Form
    13. Form 13: Corrective Action Form
    14. Form 14: Internal Audit Checklist
    15. Form 15: Laboratory Assessment Form
    16. Form 16: Assessment Finding Form
    17. Form 17: Management Review Form
    18. Form 18: Laboratory Temperature & Humidity Log

  • Meet the Author

    Best Practices from 10+ Years of Helping Labs Get Accredited

    After listening to customer feedback, Rick created an ISO 17025 quality manual template to help laboratories that couldn’t afford a consultant get accredited.

    My goal was to create a complete quality management system for ISO/IEC 17025:2017 accreditation that was easy to use and customize. So easy that my customers could customize their own quality manual and procedures without the need to hire me for consulting.

 

READY TO CREATE YOUR CUSTOM ISO 17025 QUALITY MANUAL?

(Just dedicate 1 hour a day to customizing your manual, procedures, forms, and lists)

 

Buy the Quality Manual Template Now