ISO17043 Management System
ISO17043 Management System
Run proficiency testing schemes that participants, accreditation bodies and regulators are willing to rely on.
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Written by practising auditors with 20+ years in the field.
By document type
| Category | Files |
|---|---|
| Manuals | 2 |
| Policies | 3 |
| Procedures & SOPs | 26 |
| Plans & Programmes | 1 |
| Forms & Records | 63 |
| Checklists & Audit Tools | 8 |
| Registers, Logs & Matrices | 1 |
| Training & Awareness | 2 |
| Guides & Work Instructions | 4 |
Key documents
| Reference | Document | Format |
|---|---|---|
| AGS-QM-01 | Quality Manual | Word |
| AGS-SCH-01 | PT Scheme Description | Word |
| QP-08 | Design and Planning of a PT Scheme | Word |
| QP-12 | Homogeneity and Stability Assessment of PT Items | Word |
| QP-13 | Determination of Assigned Value and Uncertainty | Word |
| F-OPN-10 | Homogeneity Assessment Report | Word |
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Overview
Proficiency testing is the external check that keeps laboratory results honest. ISO/IEC 17043 specifies the general requirements for the competence of proficiency testing providers and for the development and operation of the schemes themselves, in which participant performance is evaluated against pre-established criteria through interlaboratory comparison. It is how laboratories, inspection bodies and other conformity-assessment participants demonstrate the ongoing validity of their results and satisfy the assurance requirements set by standards such as ISO/IEC 17025. This documentation is built to the 2023 edition and covers schemes in testing, calibration, measurement, examination and inspection.
The technical heart of a provider is the scheme itself. This set works through scheme design and planning, review of participant nomination, selection of the test or measurement method, production of proficiency test items, homogeneity and stability assessment before release, determination of the assigned value and its uncertainty, and the performance criteria applied to participant results. Item handling, storage, packaging, labelling and distribution are controlled, participants receive written instructions, and collusion and falsification are treated as risks to be actively prevented rather than assumed away. Compliance is checked against the standard's own clause groups, the same lines on which accreditation bodies operating under ISO/IEC 17011, often within the ILAC arrangement, assess providers.
What this system covers
- Scheme design and planning — technical basis, participant nomination review and the testing calendar
- Production of proficiency test items, with homogeneity and stability assessment before release
- Assigned values — determining the value and its uncertainty, and the performance criteria applied to participants
- Prevention of collusion and falsification between participants
- Handling, storage, packaging, labelling and distribution of test items
- Impartiality, and confidentiality of participant identities, data and results
- Reporting to participants, participant instructions, and guidance on how a report may be used
- Clause-group compliance — general, structural, resource, process and management requirements checked separately
Who it's for
For laboratories, sector associations and independent providers running interlaboratory comparisons who need accreditation to ISO/IEC 17043 before participants and their accreditation bodies will accept the results, and for established providers launching a scheme in a new technical field. It leaves the provider with the design rationale, the item production and homogeneity evidence, and the basis of every assigned value written down and open to challenge.
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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