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ATTENTION,WHERE IT MATTERS.

The machine assembles. The analyst decides. The record proves it.

Cuegent automates the assembly and first-pass review of analytical reports inside your existing instruments, empowering your analysts to spend their hours on judgement and every judgement stays defensible, end-to-end.

Your clients pay for scientific judgement. Your analysts spend most of their day on everything around it.

Every result your lab releases is a claim someone else will act on.

Cuegent exists because that carefulness should not have to be slow. It automates the analytical layer as per your methods, records and traces every step, and always ends with human judgement.

  • Analysts get their hours back.

  • Reviewers hold tighter turnaround.

  • Labs increase volume & revenue.

  • Auditors get a chain of evidence.

Growth that does not depend on hiring!

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Developed with real analytical workflows.

Developed in active collaboration with accredited testing laboratories running food safety, cannabis, and pesticide-residue panels.

  • LC-MS/MS

  • GC-MS

  • HPLC

  • QBench LIMS

All available.

The analytical review layer.

What Cuegent does – and where it sits.

Cuegent pulls from your instruments and your LIMS, applies your methods and acceptance criteria, and produces a complete, traceable report. Analysts review exceptions. Reviewers sign with the evidence already in front of them.

How data flows through CuegentInstrument data from LC-MS/MS, GC-MS and HPLC flows through one connection into the supported tests, then into Cuegent, which ingests, processes and hands exceptions to an analyst for review and sign-off. One connection then leads to the full batch report, activity logs and LIMS delivery.INSTRUMENT DATA SOURCESSUPPORTED TESTS / ANALYTESCUEGENT PLATFORMOUTPUTSLC-MS/MSInstrument data filesGC-MSInstrument data filesHPLCInstrument data filesPotency / CannabinoidsTerpenesPesticide ResidueResidual SolventsHeavy MetalsMycotoxinsMicrobialOther Panelscuegent01 Ingest & RecogniseFiles collected. File type, compound, standardand reference identified automatically.02 ProcessCalibration curves, QC scoring, limits applied.Exceptions surfaced with a written reason.03 Review & Sign-offAnalyst reviews exceptions. Every decision,correction and sign-off stays with the analyst.Human decisionFull Batch ReportAll results, flagsand decisionsActivity LogsReport + raw data +full historyQBench LIMSSigned resultsdelivered to LIMSMore instrument workflowsPlannedHow data flows through CuegentInstrument data from LC-MS/MS, GC-MS and HPLC flows through one connection into the supported tests, then into Cuegent, which ingests, processes and hands exceptions to an analyst for review and sign-off. One connection then leads to the full batch report, activity logs and LIMS delivery.INSTRUMENT DATA SOURCESSUPPORTED TESTSCUEGENT PLATFORMOUTPUTSLC-MS/MSInstrumentdata filesGC-MSInstrumentdata filesHPLCInstrumentdata filesPotency / CannabinoidsTerpenesPesticide ResidueResidual SolventsHeavy MetalsMycotoxinsMicrobialOther Panelscuegent01 Ingest & RecogniseFiles collected. File type, compound, standardand reference identified automatically.02 ProcessCalibration curves, QC scoring, limits applied.Exceptions surfaced with a written reason.03 Review & Sign-offAnalyst reviews exceptions. Every decision,correction and sign-off stays with the analyst.Human decisionFull Batch ReportAll results, flagsand decisionsActivity LogsReport + raw data +full historyQBench LIMSSigned resultsdelivered to LIMSMore instrument workflowsPlanned

See it in action

What happens from batch to report – Platform walkthrough

Watch how Cuegent takes a real instrument batch, applies your laboratory's own rules, surfaces only the exceptions that need analyst attention, and produces a complete audit-ready report, without replacing a single step the QA process requires.

Platform walkthrough

Three principles.

Every part of the platform is built on them.

These are not feature descriptions. They are engineering decisions that carry legal and regulatory weight, and the ones a QA lead can point to in an inspection.

Automation that ends at the decision

  • Analysts see only what needs their judgement
  • No result is approved without a named reviewer
  • Parameters and thresholds remain the lab’s

Defensibility by construction

  • Full audit trail no gaps, no expiry
  • Closes manual handoffs where results can change unrecorded
  • Supports 21 CFR Part 11, ISO 17025, ALCOA+

Fits the lab as it is

  • No instrument replacement or workstation rollout
  • Configured to your existing methods and limits
  • Pilot begins with your own data, your own process

Recent writing from the lab.

Notes on defensible, review-ready analytical workflows. See all articles →

Find out if Cuegent fits your lab.

We run it through Cuegent alongside your current process and return two things: the finished batch with its complete record, and a cost assessment built from your own numbers. You see the difference on your own data before committing to anything.