THE PERFECT ISO 17025 QUALITY MANUAL TEMPLATE FOR BUSY LABS
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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
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“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)
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Easy to Customize
Just fill in the blanks to customize your quality manual. Plus, get expert tips included in the 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…
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1 Quality Manual
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12 Procedures
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14 Lists and Logs
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18 Forms
See the Full List
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Quality Manual
- Section 4.1: Impartiality
- Section 4.1: Confidentiality
- Section 5.0: Organization
- Section 6.1: General Resources
- Section 6.2: Personnel
- Section 6.3: Facilties and Environmental Conditions
- Section 6.4: Equipment
- Section 6.5: Metrological Traceability
- Section 6.6: Externally Provided Products and Services
- Section 7.1: Contract Review
- Section 7.2: Selection, Verification, and Validation of Methods
- Section 7.3: Sampling
- Section 7.4: Handling of Items
- Section 7.5: Technical Records
- Section 7.6: Evaluating Measurement Uncertainty
- Section 7.7: Ensuring the Validity of Results
- Section 7.8: Reporting the Results
- Section 7.9: Complaints
- Section 7.10: Nonconforming Work
- Section 7.11: Information Management
- Section 8.1: Management System
- Section 8.2: Management System Documentation
- Section 8.3: Document Control
- Section 8.4: Record Control
- Section 8.5: Risks and Opportunities
- Section 8.6: Improvement
- Section 8.7: Corrective Actions
- Section 8.8: Internal Audits
- Section 8.9: Management Reviews
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Procedures
- SOP 01: Managing Personnel
- SOP 02: Managing Laboratory Equipment
- SOP 03: Intermediate Checks
- SOP 04: Purchasing Products and Services
- SOP 05: Reviewing Contracts
- SOP 06: Validating Methods
- SOP 07: Handling Items
- SOP 08: Ensuring Validity of Results
- SOP 09: Handling Complaints
- SOP 10: Handling Nonconforming Work
- SOP 11: Conducting Internal Audits
- SOP 12: Evaluating Measurement Uncertainty
Lists
- List 01: Organization Chart
- List 02: Master Document List
- List 03: Distribution List
- List 04: Equipment List
- List 05: Training Log
- List 06: Qualification List
- List 07: Supplier List
- List 08: Purchase Log
- List 09: Method Validation Log
- List 10: PT/ILC Plan
- List 11: Complaint Log
- List 12: LIMS Log
- List 13: LIMS Error Log
- List 14: Risks and Opportunities List
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Forms
- Form 01: Impartiality Agreement
- Form 02: Confidentiality Agreement
- Form 03: Competence Requirements Worksheet
- Form 04: Employee Training Log
- Form 05: Employee Evaluation Form
- Form 06: Purchase Order
- Form 07: Product/Service Inspection Form
- Form 08: CMethod Validation Form
- Form 09: Complaint Form
- Form 10: Handling Complaints Handout
- Form 11: Nonconformance Form
- Form 12: Customer Survey Form
- Form 13: Corrective Action Form
- Form 14: Internal Audit Checklist
- Form 15: Laboratory Assessment Form
- Form 16: Assessment Finding Form
- Form 17: Management Review Form
- Form 18: Laboratory Temperature & Humidity Log
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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)