Quality management without the binders
Corrective actions, document control, training records, and audit trails — built into the same system that runs your testing, not bolted on beside it.
Corrective actions
A staged workflow — Problem → Impact → Containment → Root Cause → Corrective Action → Effectiveness Review — with tasks and approvals at every stage. Print completed CARs for auditor review.
Try the free corrective action templateDocument control
Version-controlled documents with revision history, classifications, and organization — so the current procedure is always the one people find, and superseded revisions stay traceable.
Try the free SOP templateTraining records
Link training to specific staff members, attach training videos, and keep records current — so you can show exactly who was qualified to run which test, and when.
Try the free training matrixAudit trails
Every change to your lab data is logged automatically: who, what, when, and before/after values. Download audit reports when the assessor asks — no reconstruction required.
Review workflows
Requester and lab manager reviews of testing exist as explicit, trackable tasks — the steps ISO/IEC 17025 requires, built into every job instead of remembered by heart.
Calibration traceability
Calibration records with certificates, expiration tracking, and instant impact tracing when equipment fails its as-found condition — you know what's affected before your auditor does.
“It was easily implemented and is easy to use. It is an indispensable tool to help our lab maintain ISO compliance. All your documents are in one location; test results, equipment maintenance and calibration records, corrective and preventive actions, and anything else you need for your auditors. It can be customized to your needs.”
Pursuing or holding ISO 17025? See how accredited labs use LIMSey
Be audit-ready as a side effect
Quality records that write themselves while your lab does the testing.