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ISO/IEC 17025 Laboratory Audit Checklist

A clause-by-clause ISO/IEC 17025:2017 internal audit checklist for testing and calibration laboratories, with an equipment and calibration log.

A working kit for internal audits of a testing or calibration laboratory against ISO/IEC 17025:2017. The checklist follows the standard from clause 4 to clause 8, so each finding can be traced to a requirement, and the log gives you the equipment and calibration records that auditors and assessors ask for first.

What is inside

ISO/IEC 17025 Laboratory Audit Checklist — 114 checks in 11 sections across clauses 4 to 8: impartiality and confidentiality, structure, resources, the laboratory process from contract review to the report, and the management system. Each check is a statement you can find evidence for, with Yes / No / N/A boxes and space for notes.

Equipment and Calibration Log — four templates: an equipment register, a calibration and intermediate check schedule, a calibration record and an out-of-tolerance / nonconforming work record.

Both documents as a designed, print-ready PDF and as an editable Word file.

Who it is for

Laboratory managers, quality managers, technical managers and internal auditors in testing and calibration laboratories — whether you are preparing for an accreditation assessment, keeping an accredited laboratory in shape, or running an in-house laboratory that wants results people can rely on.

How to use it

Audit the technical work as well as the paperwork. Pick a few recent reports or certificates and trace each one backwards: the contract review, the method and its verification or validation, the person and their authorisation, the equipment and its calibration, the environmental conditions, the raw data, the uncertainty, the quality control results and the review of the report. Witness a test or calibration being done. Use the checklist to make sure nothing is missed. For every No, write a nonconformity that states the requirement, the evidence and why it does not conform.

This kit covers the standard only. Accreditation bodies and regulators publish their own requirements and policies, for example on proficiency testing, metrological traceability and the use of accreditation symbols — check the ones that apply to your laboratory, and check which edition of the standard applies to you.

What is in the kit

  • ISO/IEC 17025 Laboratory Audit Checklist (PDF)114 checks in 11 sections across clauses 4–8 of ISO/IEC 17025:2017, with Yes / No / N/A boxes, space for evidence and a score table.
  • Equipment and Calibration Log (PDF)Four templates: equipment register, calibration and intermediate check schedule, calibration record, and out-of-tolerance / nonconforming work record.
  • ISO/IEC 17025 Laboratory Audit Checklist (editable Word)The same document in Word, so you can adapt it and fill it in on screen.
  • Equipment and Calibration Log (editable Word)The same document in Word, so you can adapt it and fill it in on screen.

A look inside

The first pages of ISO/IEC 17025 Laboratory Audit Checklist (PDF). The full document downloads from the list above.

ISO/IEC 17025 Laboratory Audit Checklist — preview of page 1ISO/IEC 17025 Laboratory Audit Checklist — preview of page 2

Next step

Learn to use it properly — with a certificate

The documents tell you what to check. These courses teach you how to audit and implement it, online and at your own pace.

Questions people ask

Is the ISO/IEC 17025 Laboratory Audit Checklist really free?

Yes. There is no payment and no trial. Tell us your name, work email and company once, and every document in the Free Zone is yours to download.

What format are the documents in?

This kit has 4 documents in PDF and DOCX format. The Word, Excel or PowerPoint files are fully editable, so you can adapt them to your organisation.

Can I use it inside my company?

Yes. The licence covers one organisation with unlimited internal use — print it, share it with colleagues and adapt it. Please do not resell it or republish it as your own.

Does this make us compliant with ISO/IEC 17025?

No document can do that on its own. It is a practical working tool to help you prepare, check and improve. Conformity with ISO/IEC 17025 is decided by an audit of your actual system, and the standard itself remains the authoritative text.

Do you offer training on this topic?

Yes. Skedmia runs online courses with certificates on the standards and topics these kits cover — the matching courses are listed on this page.

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