Lab Relations
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LabRelations for QC Labs

QC is precision work under release pressure. Methods are locked, instruments are validated, and every result carries a name, a timestamp, and a defensible trail. LabRelations builds LIMS for that work: sample registration, testing, instrument data, batch genealogy, stability, and CoA generation in one place. QMS sits alongside for SOPs, training, deviations, OOS investigations, and CAPA.

The analyst works in software designed for the bench, and QA works in software designed for quality. They share data where it counts (an OOS opens straight from the result that triggered it, an SOP read by an analyst is logged the same way as the test itself), but each system stays focused on the team using it.

What QC teams use LabRelations for

LIMS for the bench, QMS for the quality work that wraps it. Used independently, connected where it counts.

What does the LIMS handle on a typical day? +

Sample registration, scheduling, method execution, instrument data capture, batch genealogy, stability planning, inventory, and CoAs. Analysts work one queue. Released results flow into the batch record without re-typing.

What does QMS add on top of that? +

SOPs, training, deviations, change control, supplier qualification, and CAPA. The records auditors ask for are already organised and connected to the batch they relate to.

How does it handle OOS, OOT, and investigations? +

An OOS opens directly from the result that triggered it. Sample, method, batch, and instrument context travel with the investigation through root cause and CAPA. Unrelated samples keep moving, so the lab doesn't grind to a halt around one investigation.

How are methods and specifications kept under control? +

Methods, specifications, calculations, and edit checks are version-controlled. The right version applies to the right batch automatically. Changes go through a controlled change with electronic approvals before they're live.

How does it handle 21 CFR Part 11, EU GMP Annex 11, and ALCOA+? +

Audit trails on every action. Electronic signatures on the actions that need them. Role-based access by site, lab, and role. The audit trail is exportable for inspectors and filterable by user, time, sample, and batch.

What about validation when we configure things? +

Configuration in the UI doesn't break validation. The validation envelope covers the configuration model, so workflow, field, and approval changes are controlled changes, not code releases.

What kind of support do we get? +

A mix of people who've actually worked in the industry supported by technical people for configuration needs inside the platform itself.

Let's get you started

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  • LIMS for the bench, QMS for the quality work
  • Direct instrument integrations
  • 175+ features and counting
  • Configurable without breaking validation
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