ISO/IEC 17025:2017 Management System
ISO/IEC 17025:2017 Management System
Every result your laboratory releases has to hold up in front of the customer, the regulator and the accreditation assessor.
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Written by practising auditors with 20+ years in the field.
By document type
| Category | Files |
|---|---|
| Manuals | 2 |
| Policies | 2 |
| Procedures & SOPs | 26 |
| Plans & Programmes | 3 |
| Forms & Records | 75 |
| Checklists & Audit Tools | 7 |
| Registers, Logs & Matrices | 1 |
| Job Descriptions & Organisation | 1 |
| Training & Awareness | 4 |
| Guides & Work Instructions | 7 |
Key documents
| Reference | Document | Format |
|---|---|---|
| QM-01 | Quality Manual | Word |
| CHK-06 | ISO-IEC 170252017 Self-Assessment - Gap-Analysis Checklist | Word |
| QP-11 | Procedure for Evaluation of Measurement Uncertainty | Word |
| QP-06 | Procedure for Measurement Traceability and Calibration | Word |
| QP-09 | Procedure for Method Verification and Validation | Word |
| F-QCD-04 | Uncertainty of Measurement Calculation Sheet | Word |
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Overview
A laboratory is accredited on three words — competence, impartiality and consistency — and ISO/IEC 17025:2017 is where they are given operational meaning. It applies to any organisation performing laboratory activities, whatever its size or scope, including laboratories inside a larger parent. Its requirements fall into general, structural, resource and process groups: impartiality and confidentiality; organisation and responsibilities; personnel, facilities, equipment, metrological traceability and external providers; then method selection and validation, sampling, measurement uncertainty, validity of results, reporting and nonconforming work. This system follows that structure.
The technical weight sits where assessors concentrate. Measurement uncertainty is evaluated on calculation sheets and stated on reports; metrological traceability is established and defended; calibration periodicity is scheduled and supported by intermediate checks between calibrations; and decision rules govern any statement of conformity placed against a specification. Test request and sampling sheets are drafted for water and waste water, process stack, ambient air, noise and sludge, and a schedule of activities defines the scope of accreditation claimed. The management system may follow the prescriptive route or align with ISO 9001, and accreditation bodies operating under ISO/IEC 17011, generally within the ILAC arrangement, assess against it.
What this system covers
- Measurement uncertainty — evaluation, calculation and how uncertainty is expressed on a report
- Metrological traceability and calibration — calibration periodicity, intermediate checks and equipment history
- Method verification and validation, and the controlled introduction of a new method
- Decision rules and statements of conformity against a specification
- Sampling and item handling — sheets for water, waste water, stack, ambient air, noise and sludge, plus receipt, storage and item integrity
- Validity of results — internal quality checks against defined acceptance criteria, and control of nonconforming work
- Impartiality, confidentiality, laboratory environmental conditions and verification of reports before release
Who it's for
Aimed at the quality or technical manager of a testing or calibration laboratory — environmental testing laboratories in particular, given the sampling coverage — facing a first accreditation assessment, a reassessment or an extension of scope onto new methods. The result is a laboratory whose uncertainty budgets, traceability chain, method validation records and pre-release report checks live in one coherent set instead of being reassembled whenever an assessor is booked.
Everything you get
Every toolkit gives you a full set of working documents for your standard, ready to edit and use.
Native Microsoft files. Add your logo and adapt every document to how you work.
Your full toolkit arrives as a ZIP the moment payment clears.
One purchase covers everyone in your organisation. No per-seat fees.
Built by people who run real audits, so the content matches what assessors check.
One payment, perpetual licence for your organisation. No subscriptions, no renewals.
Full refund if your files are faulty, incomplete or not as described and we can't put it right
Frequently asked questions
What exactly do I receive?
A downloadable ZIP containing the full set of ready-to-use documents for this toolkit — manuals, procedures, forms, records, checklists, guidance and training material, all in editable Word and Excel format. The exact document count is shown at the top of this page.
Are the documents really editable?
Yes. Every file is native Microsoft Word or Excel — no locked PDFs. Add your logo, change wording, and tailor the content to your organisation. The toolkit is yours to keep and reuse.
Does this certify my organisation?
No. These are documentation toolkits aligned to the relevant standard to help you prepare. Certification itself is issued by an accredited certification body after their audit. Our toolkits give you a strong, audit-ready starting point.
How is it delivered?
Instantly and digitally. There's no physical shipment — you download the files right after payment and receive a backup link by email.
Do I get updates?
Yes. If we revise this toolkit, you're entitled to the updated version at no extra cost — just contact us with your order details.
What is your refund policy?
These are digital products, so once a toolkit has been downloaded we cannot take it back. If you have not downloaded yet, contact us and we will cancel the order and refund you in full. We also refund in full if the files are damaged, incomplete, or not what the product page described.
Cannot find your standard?
Tell us which scheme you work to. We will point you to the right toolkit.
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