Upload your quality manual, procedures and records. The toolkit reads them against every clause of ISO/IEC 17025:2017 and tells you, requirement by requirement, what your documents do not yet demonstrate — and names the document it looked in.
No card for the trial. Your registers stay readable and exportable even if you never pay.
All three read your own documents and your own risk matrix. None of them invent a finding they cannot point at a document for.
Every clause of the standard, checked against every document you have uploaded — not a sample.
Paste the assessor's finding. Get it back mapped, analysed and ready to answer.
Clause 8.5 handled properly: risks scored to a residual, on the matrix in your own quality manual.
Quality manual, procedures, forms, records, calibration certificates. Word, PDF, Excel, scans. Nothing has to be reformatted first.
Every requirement is judged against those documents and marked met, partly met or not demonstrated — with the reason and the source document named.
Turn findings into non-conformances, clear them with root cause and corrective action, and export the lot. Every edit is recorded and cannot be rewritten.
No per-report charge, no per-audit charge, no minimum term beyond the one you pick. Run the gap audit as often as you like.
A numbered quotation on our letterhead, with banking details and a purchase-order reference, in your inbox in under a minute. No call, no sales follow-up.
Your procurement officer will ask. These are the answers, and they are checkable.
Every record carries the laboratory it belongs to, and the database itself refuses to return another laboratory's rows. That rule lives below the application, so it holds even if the application is wrong.
Who changed what, and when, written by the database rather than the application, and append-only. Nobody can add a false entry or remove a true one — not your administrator, and not us.
Support access needs a written reason, and that reason is written into your own change history before anything is returned. You see who looked, when and why, beside your own edits. It is read-only.
If a licence lapses, your registers remain readable and exportable. Only new analysis stops. You are never locked out of your own quality records to force a renewal.
What you upload stays in your laboratory's own storage and is read only to answer that laboratory's audits, clearances and risk assessments. Not pooled, not shared between customers, not used to train anything.
The requirements are our own plain-language statement of what each clause obliges you to demonstrate. ISO/IEC 17025:2017 is copyrighted by ISO and is not distributed with this product. You need your own licensed copy, as you would for any assessment.
No, and it does not pretend to. A gap finding means a requirement is not demonstrated in the documents you provided — it does not mean your laboratory does not do it. Risk scores are proposals for your technical judgement. Every finding names the document it came from so you can check it yourself.
Yes. The standard is copyrighted by ISO and is not supplied with this product. If you hold a licensed copy you may upload it into your own library, where it stays.
New analysis stops. Everything you produced stays readable and exportable. Nothing is deleted, and nothing is held hostage.
Ask for a quotation and pay by EFT. Most laboratories buy this way: we issue a quotation against your purchase order, you pay, and the licence is switched on the day the payment lands.
A laboratory licence covers up to five users on one site, with further sites added to the same licence. The individual licence is for one consultant working across their own client laboratories.
Database, sign-in and file storage are hosted in Ireland (European Union); the site is served through Netlify. Text and images from your documents are sent for analysis at the moment you run one. Nothing else leaves the system.
Upload your quality manual this afternoon and know by this evening what your next assessment is going to find.