Chromatography LIMS for QC testing against spec
HPLC, UPLC, GC, and ion chromatography workflows with CDS integration, system suitability enforcement, and specification evaluation built into every result.
Chromatography LIMS for QC testing against spec
HPLC, UPLC, GC, and ion chromatography workflows with CDS integration, system suitability enforcement, and specification evaluation built into every result.
THE PROBLEM
A QC chromatography lab lives between the CDS and the LIMS, and the gap between them is where the work goes. Sequences get built by hand, results get transcribed or half-integrated, and system suitability is checked by someone reading a printout before the batch can move.
Every test has a spec, every spec has a version, and the LIMS usually knows the spec while the CDS knows the result. Reconciling them at release is manual, and an out-of-spec investigation starts by pulling the paper trail from both.
Labbit integrates with Empower and OpenLab, evaluates every result against the controlled spec automatically, and enforces USP 621 system suitability before results are accepted. OOS results route into investigation with the full chromatographic context attached. QC labs like Grant Industries and Momentive Technologies run on Labbit.
PRE-CONFIGURED WORKFLOWS
Built visually in BPMN, adapted to your lab, and changed without a vendor release.
Instruments and platforms
Does Labbit integrate with Empower and OpenLab CDS?
Yes. Sequences are generated from the LIMS worklist and results return to the sample record. System suitability results are captured and enforced before result acceptance.
How does Labbit handle specifications and versions?
Specifications are controlled entities with version history. Every result evaluates against the spec version in force at the time of test, and spec changes are tracked.
What happens on an out-of-specification result?
The result flags, the sample routes into an OOS workflow, and the investigation record links to the chromatographic run, reagent lots, and column history.
Is Labbit suitable for GMP QC release?
Yes. 21 CFR Part 11 electronic records and signatures, role-based review, and complete data integrity controls across the test lifecycle.
SEE IT ON YOUR ASSAYS
Bring an assay your team runs today. We’ll show you how it’s configured, executed, and reviewed.