ISO/IEC 17025 guide
How to verify ISO 17025 accreditation and a laboratory's scope, and spot a false claim
Clause by clause: ISO/IEC 17025:2017 requirements: every clause explained →
How to confirm that a laboratory's ISO/IEC 17025 accreditation is genuine, current and covers the result you rely on: where to check, how to read the schedule, the signs of a false or misleading claim and what to do when one fails.
Key points
- To verify ISO 17025 accreditation, confirm three things: the accreditation body is recognised, the laboratory appears on that body's public register, and the current schedule lists the exact test or calibration you rely on.
- Accreditation belongs to a scope, not to a laboratory as a whole. A genuine accreditation says nothing about work that is missing from the schedule.
- A "17025 certificate" from a certification body, a consultant or the laboratory itself is not accreditation, and no register will show it.
- When a claim fails, ask the accreditation body directly, decide what to do about results you have already used, and record the evaluation of that provider.
What exactly are you verifying?
"Is this laboratory accredited?" can be answered yes while the answer you need is no, because ISO/IEC 17025 accreditation is granted by an accreditation body for a defined list of tests or calibrations, with their methods, ranges and sites, published on a schedule. A food laboratory accredited for moisture and fat may run your pesticide screen in the same building, unaccredited.
So the real question has three parts. Is the body that granted the accreditation itself recognised? Is the accreditation current today, not merely on the date printed on a PDF someone e-mailed you? And does the schedule cover the specific result you are about to rely on, at the range, site and method version the laboratory actually used?
The accreditation body works to ISO/IEC 17011, sends a lead assessor and technical assessors into the laboratory and watches the work being done before it decides. A document that skipped that process is worth little, however official it looks. If you are unsure how the schedule itself is built, our guide to the ISO/IEC 17025 scope of accreditation explains the lines it contains.
Where to verify ISO 17025 accreditation
Use independent sources, in this order, never only documents the laboratory supplies.
1. Global ACI's list of recognised accreditation bodies
Since 1 January 2026, international recognition of accreditation runs through Global ACI (Global Accreditation Cooperation Incorporated), which brought together ILAC and IAF. Its Multilateral Recognition Arrangement replaced the ILAC MRA, and accreditations issued under the ILAC MRA continue to be recognised while arrangements move across. Global ACI publishes the accreditation bodies it recognises, filterable by economy and scope. Confirm that the body named on the laboratory's documents appears there for testing or calibration, whichever you need.
2. The accreditation body's own register
A recognised body publishes the organisations it accredits, with each one's certificate and schedule. Search for the laboratory by name, check the entry is for the same legal entity and address, and open the schedule from the body's site rather than from an attachment. National bodies such as UKAS in the United Kingdom, NABL in India, the Philippine Accreditation Bureau, EIAC in Dubai or NATA in Australia are typical places to look, depending on where the laboratory operates.
3. The laboratory's certificate and schedule, cross-checked
Ask the laboratory for its accreditation certificate and the current issue of its schedule. Compare both with what the body publishes: name, site, the laboratory's reference number with the body, the standard (ISO/IEC 17025:2017) and the issue date of the schedule.
4. The report in your hands
Finally, check the report or calibration certificate you received against the schedule. Accreditation bodies set rules on how their symbol may appear and how results outside the scope are to be identified, so ask the laboratory which results on the report are covered, and read the answer against the schedule yourself.
ISO 17025 accreditation verification checklist
Work through these checks for every laboratory, calibration provider or reference material supplier whose results feed decisions you have to defend.
| Check | Where to confirm it | Pass | Warning sign |
|---|---|---|---|
| The accreditation body is recognised | Global ACI list of recognised bodies | Listed for testing or calibration, as relevant | Body missing, or listed only for other scopes |
| The laboratory is accredited now | The body's register | Entry current, same legal entity and site | No entry, or status shown as suspended or withdrawn |
| The standard is ISO/IEC 17025 | Certificate and register entry | ISO/IEC 17025:2017 named | ISO 9001 or a management system standard instead |
| Your test or calibration is on the schedule | Current schedule from the body's site | Item, property or quantity and method listed | Similar work listed, yours absent |
| Range and capability fit your need | Schedule ranges and stated capability | Your value sits inside the range | Your value outside, or no range stated |
| The work was done at an accredited site | Sites on the schedule | Report site matches | Work subcontracted or moved to an unlisted site |
| The report identifies accredited results | Report read against schedule | Covered results clearly identifiable | Accreditation symbol on a report of unlisted work |
Keep a dated record of each check; if your organisation is accredited or certified, it is also evidence of how you control external providers.
Signs of a fake or misleading ISO 17025 claim
Forgeries exist, but most problems are claims that are technically true and practically misleading.
- "Certified to ISO 17025". Laboratories are accredited, not certified. A certificate issued by a management system certification body, which works to ISO/IEC 17021-1, or by a consultant, is not accreditation and will not appear on any accreditation body's register.
- "ISO 17025 compliant". A self-declaration: nobody independent has watched the work.
- An ISO 9001 certificate offered instead. It shows a quality management system, not technical competence for a named test.
- An accreditation body you cannot find. An official-sounding name missing from Global ACI's list deserves a hard look.
- A schedule that is old, partial or not the body's. A PDF with an early issue date may no longer match what the body publishes; scopes are extended, reduced and reissued.
- The right laboratory, the wrong scope. The most common case in practice: a genuinely accredited laboratory issues a report on work that is not on its schedule.
- The ISO logo used as proof. ISO writes the standard; it does not certify anyone or issue certificates, and it does not permit its logo to be used in connection with certification.
- A promise measured in days. If a provider offered the laboratory "accreditation" in ten days, it was not ISO/IEC 17025 accreditation. Validation, uncertainty and proficiency testing alone take longer.
What to do when an accreditation does not check out
Start with a question, not an accusation. Write to the laboratory, name the discrepancy you found and ask for its explanation and the current schedule. Many gaps turn out to be a recent scope extension or a report that should have marked a result as unaccredited.
If the answer does not settle it, contact the accreditation body. It can confirm whether an accreditation exists, whether it is current and what it covers; only the body can do that. If a document appears forged, tell the body.
Then deal with the consequences on your side:
- Identify the results already used from that provider and what depended on them.
- Decide, with a recorded rationale, whether to repeat the work elsewhere.
- Update your approved provider records and selection criteria.
For an accredited laboratory this matters twice: ISO/IEC 17025 expects metrological traceability of results and control of externally provided products and services, so a calibration certificate from a provider whose scope does not cover the instrument or range can undermine your own traceability chain. Our guide to equipment, calibration and metrological traceability covers how that chain is built.
Your own laboratory: make your accreditation easy to verify
The checks above are the ones your customers, regulators and tender panels will run on you. Laboratories that pass them easily link their website to the body's copy of the schedule, say in quotations which tests are inside the accredited scope, mark unaccredited results plainly and never describe themselves as "certified". Keeping the scope current matters as much as winning it; see ISO/IEC 17025 surveillance and reassessment.
How Sterling prepares laboratories
An accreditation that survives any buyer's check, because the assessment behind it was real.
Sterling does not accredit and never offers a shortcut around the accreditation body. Our expert and experienced consultants build the management system and technical evidence with your staff and prepare you for a full on-site assessment with witnessing. Effivity holds the management system records from the first workshop. We ensure successful accreditation for our clients.
Book a free discovery callVerifying ISO 17025 accreditation: questions buyers ask
A laboratory sent us its accreditation certificate but no schedule. Is that enough?
No, the certificate alone is not enough, because it confirms that an accreditation exists but not what it covers. Download the current schedule from the accreditation body's website and check that your test or calibration, range and site are on it.
The laboratory is accredited, but not for the test we need. Can we accept its report?
You can accept it only as an unaccredited result, and you should decide knowingly whether that is good enough for the purpose. If a regulator, customer or contract requires accredited results, choose a laboratory whose schedule lists the work.
Do reports that carry the ILAC MRA mark still count now that Global ACI has replaced ILAC?
Accreditations issued under the ILAC MRA continue to be recognised while the arrangements move to the Global ACI MRA, and the ILAC MRA mark was transferred to Global ACI. How long the old mark may appear on new reports is set by the transition rules, so ask the accreditation body if it matters to you.
How often should we re-check a calibration provider's or testing laboratory's accreditation?
Re-check before first use, at every re-approval of the provider and whenever you order work outside your usual tests or ranges. Accreditations are kept under surveillance and can be reduced, suspended or withdrawn between your checks.
Our supplier's medical laboratory says it is accredited to ISO 15189, not ISO/IEC 17025. Is that a problem?
Not necessarily, because ISO 15189 is the accreditation standard for medical laboratories. Verify it the same way: a recognised body, a current register entry and a schedule that lists the examinations you need.
Can Sterling confirm whether a laboratory is accredited?
No, only the accreditation body can confirm an accreditation and its scope. Sterling can show your team how to build these checks into supplier evaluation.
More ISO/IEC 17025 guides
Every guide in the ISO/IEC 17025 series is written for one question and links back to the hub for the whole picture.
- ISO/IEC 17025 accreditation process, step by step
- ISO 17025 assessor questions
- ISO 17025 accreditation in Australia
- ISO/IEC 17025 accreditation cost: what moves the price
- ISO/IEC 17025 documentation: what you need
- ISO/IEC 17025 internal audit: the technical clauses
- Measurement uncertainty under ISO/IEC 17025: a budget you can defend
- Method verification and validation under ISO/IEC 17025
- ISO/IEC 17025 requirements explained, clause by clause
- ISO 17025 accreditation in the UK
- ISO 17025 timeline
- ISO 17025 training
Keep exploring
Explore more about ISO/IEC 17025
Watch a video on how to implement ISO 17025 here.
Watch a video on ISO 17025 requirements here.
ISO/IEC 17025 resources
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