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ISO/IEC 17025 guide

Choosing an ISO 17025 accreditation body: Global ACI recognition, technical fit and how to compare offers

Clause by clause: ISO/IEC 17025:2017 requirements: every clause explained →

How to choose an accreditation body for ISO/IEC 17025: what the body does, what Global ACI recognition means since it replaced the ILAC MRA, national bodies by market, the technical questions to ask, how to compare offers and the warning signs.

  • Updated September 2026
  • 8-minute read
  • Part of the ISO/IEC 17025 hub

Key points

  • Only an accreditation body working to ISO/IEC 17011 can accredit a laboratory to ISO/IEC 17025. A "17025 certificate" from a certification body or a consultant is not accreditation.
  • International recognition now runs through the Global ACI arrangement, which replaced the ILAC MRA on 1 January 2026. Check the body's standing for testing or calibration on the Global ACI list yourself.
  • Most laboratories apply to their national body, and in some places local regulation leaves little choice. Confirm who must accept your results before you compare bodies.
  • Ask every body the same questions: technical assessors for your disciplines, assessment days, witnessing, fees across the whole cycle and its deadlines for closing findings. Sterling does not accredit; the choice of body is yours.

What does an ISO 17025 accreditation body actually do?

An accreditation body is the organisation that decides whether your laboratory is competent for a stated list of tests or calibrations. It works to ISO/IEC 17011:2017, the standard for bodies that accredit conformity assessment bodies, and it has no role in running your laboratory.

It reviews your application and documents, then sends a lead assessor and technical assessors who watch selected tests or calibrations and examine the evidence behind the numbers. The body's committee or council then takes the decision. If accreditation is granted, the body publishes a schedule naming the methods, ranges and sites covered, then keeps checking through surveillance and reassessment.

The choice matters: the body's recognition decides where your results are accepted, and its assessors will return for years. The full sequence from application to decision is set out in our guide to the ISO/IEC 17025 accreditation process.

Global ACI recognition: what it means for a laboratory

On 1 January 2026 ILAC and IAF were brought together in a single organisation, Global Accreditation Cooperation Incorporated, known as Global ACI. Its Multilateral Recognition Arrangement (MRA) replaced the ILAC MRA, under which laboratory accreditation had been recognised internationally, and the IAF MLA used for certification bodies.

The arrangement exists to reduce technical barriers to trade. Each signatory accepts the accreditations of the others as equivalent to its own, except where regulation or law says otherwise.

Three points follow:

  • Recognition is by scope. A body can be a signatory for certification or inspection without being one for testing or calibration. Check the scope that matches your laboratory activities.
  • Existing accreditations carry over. A body whose website still cites the ILAC MRA is not automatically a concern; ILAC-era accreditations remain recognised during the transition.
  • The list is the authority. Use Global ACI's published list of recognised bodies, not a brochure logo.

National body or another signatory?

Most laboratories apply to their own country's accreditation body: its assessors share your language, local regulators know it and travel stays local. In some markets the question is settled for you. In Dubai, for example, EIAC states that registration is mandatory for Dubai-based laboratories under local regulations, while accreditation outside Dubai is voluntary. In the European Union, national accreditation bodies are designated by their governments under Regulation (EC) No 765/2008.

A laboratory may look abroad when its customers sit in another market or the national body lacks assessors for a specialised discipline; first ask whoever relies on your results whether they accept a foreign body.

The table shows what national bodies in Sterling's main markets say about themselves. We assert no body's current Global ACI standing: in September 2026 several did not appear on the list as we viewed it, and some still cite ILAC-era arrangements.

MarketAccreditation bodyWhat the body states about itselfCheck before applying
United KingdomUKASThe national accreditation body appointed by government; states that it is a Global ACI MRA signatoryIts testing or calibration standing on the Global ACI list
PhilippinesPAB, Department of Trade and IndustryCites the ILAC and APLAC arrangements for testing and calibrationIts current Global ACI recognition status; not stated here
IndiaNABL, a constituent board of the Quality Council of IndiaAccredits testing and calibration laboratoriesIts current Global ACI standing; not seen on the list as viewed
United Arab EmiratesEIAC, Government of DubaiCites ILAC MRA, IAF MLA, APAC and ARAC signatory statusIts Global ACI standing, and any local registration rule
GCC statesGAC, the Gulf accreditation body based in RiyadhAccredits to ISO/IEC 17025:2017; cites the ILAC and IAF arrangementsIts Global ACI standing for your scope
SingaporeSAC, through its SINGLAS schemeCites ILAC MRA and APAC MRA membershipIts Global ACI standing for your scope
NetherlandsRvADesignated in 2010 as the Dutch national body; a member of EA, the European accreditation networkIts Global ACI and EA standing for laboratories
AustraliaNATAAccredits testing and calibration laboratoriesIts current Global ACI standing; not seen on the list as viewed

Can the body assess your tests and calibrations?

Recognition shows the body is credible, not that it has technical assessors for each discipline you apply for. Ask:

  • Does it already accredit laboratories for these methods or ranges, with published schedules to show it?
  • Who will act as technical assessor for each discipline, and how soon are they available?
  • Which tests or calibrations will be witnessed?
  • How must calibration capability and uncertainty be expressed on the schedule?
  • Does the body allow a flexible scope, and under which of its own rules?
  • What does its proficiency testing policy require before grant? NABL, for instance, asks applicants to take part successfully in at least one scheme first.

How to word the scope you apply for is covered in our guide to the ISO/IEC 17025 scope of accreditation, and planning scheme participation in the guide to proficiency testing.

What the application pack should tell you, and three offers compared

Ask each body for its application pack and fee schedule before you apply, and collect the same facts from each: application and document review charges, any pre-assessment, lead and technical assessor days and their basis, witnessing, travel, annual and surveillance charges, the reassessment cycle, the deadline for closing findings and the decision time. How these lines add up is explained in our guide to ISO/IEC 17025 accreditation cost.

Cycles and deadlines genuinely differ. UKAS describes a first surveillance visit six months after grant, annual surveillance and full reassessment every fourth year, with about 12 weeks to evidence mandatory findings. NABL describes annual surveillance, reassessment every two years and 30 days for corrective action. EIAC grants accreditation for three years.

An illustrative comparison for a single-site calibration laboratory:

What the offer showsOffer A: national bodyOffer B: foreign signatoryOffer C: "17025 certificate"
Who issues itAccreditation body working to ISO/IEC 17011Accreditation body working to ISO/IEC 17011A certification body or consultancy
Global ACI listListed for calibrationListed for calibrationNot on the list as a laboratory accreditor
Technical assessorsNamed discipline, localFlown in; dates set by availabilityOne auditor, no discipline stated
WitnessingSelected calibrations witnessedSelected calibrations witnessedDocument review only
OutcomePublic schedule of methods and rangesPublic schedule of methods and rangesA certificate on no accreditation register
Local regulatorAcceptsAsk before applyingNot accepted as accreditation
VerdictThe default choiceViable where customers or the discipline require itDecline

Warning signs when choosing an accreditation body

  • A certificate in days. Accreditation follows validated methods and records built up over normal work, never a fortnight.
  • No technical assessors and no witnessing. A document check alone cannot establish competence to perform a test or calibration.
  • No public schedule. Accreditation without a published scope gives your customers nothing to verify.
  • A body you cannot find on the Global ACI list or in a national directory.
  • A consultant who issues the accreditation too. Consultants prepare laboratories; only accreditation bodies accredit.

How to check an existing accreditation and its scope is covered in our guide to verifying a laboratory's ISO/IEC 17025 accreditation.

Where Sterling stands

Sterling does not accredit. The body you choose assesses and decides; our part is an informed choice and a prepared laboratory.

How Sterling helps you choose

The right body for your scope, and a laboratory ready for its assessors.

In a Sterling ISO/IEC 17025 engagement the accreditation route is settled at the gap analysis. We confirm who must accept your results, check each candidate body's recognition and technical coverage, compare their fees and prepare the application. Your management system runs in Effivity, included with the engagement, at no additional cost. We ensure successful accreditation for our clients, with the assessment and the decision left to the independent accreditation body.

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Choosing an ISO/IEC 17025 accreditation body: questions buyers ask

Does accreditation under the ILAC MRA still count now that Global ACI exists?

Yes. Accreditations issued under the ILAC MRA continue to be recognised while arrangements move to the Global ACI MRA; ask your body how its transition stands.

Our certification body offers ISO 17025 as well. Is that the same as accreditation?

No. Certification bodies work to ISO/IEC 17021-1 and certify management systems; they cannot accredit a laboratory, and a "17025 certificate" from one appears on no accreditation register.

How long does the accreditation body take once we apply?

It depends on the body and your readiness. NABL speaks of about 90 days for a well-prepared laboratory and EIAC of one to three months; the whole programme, including preparation, usually takes six to twelve months. See our ISO/IEC 17025 timeline guide.

Should we ask the accreditation body for a pre-assessment?

Where offered, often yes. UKAS and NABL, among others, offer an optional pre-assessment that shows how ready you are before the initial assessment; plan its cost and time in.

Do the assessors decide whether we are accredited?

No. The assessment team reports its findings and checks your corrective action; the decision is taken by the body's committee or council. The on-site stage is described in our guide to the ISO/IEC 17025 assessment.

Can the same body accredit our medical or inspection work too?

Often, yes. GAC, for example, accredits to ISO 15189 and ISO/IEC 17020 as well as ISO/IEC 17025. Check that the body's recognition covers each scheme you need.

ISO/IEC 17025 implementation

ISO/IEC 17025 requirements

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