Scientist working at a microscope in a laboratory
PHARMA & LIFE SCIENCES · MES · LIMS · QMS · ERP

Xura for pharma. Your data team for batch, quality, and compliance.

Your batch records, lab results, deviations, and inventory live in systems that don't talk to each other. Xura connects them into one knowledge graph, answers the question in plain language, and runs the follow-up — no new dashboards to build, no report to wait on.

Private beta · your data stays in your infrastructure

The problem

The answer exists. It's just trapped across five systems.

Every yield question, every audit prep, every stock-out starts with someone stitching together exports by hand. It's slow, and by the time the report lands, the moment has passed.

Yield drops go unexplained for days. Batch data sits in the MES, quality in the LIMS, and nobody can correlate them fast enough to act on the next batch.

Audit prep eats weeks. Pulling open deviations, overdue CAPAs, and change controls into one view means chasing owners across QMS spreadsheets.

Raw material stock-outs stall production. Reorder points don't account for the actual production plan, so key starting materials run short at the worst time.

QC release is a black box. "Which batches are waiting, and on what?" takes a round of emails instead of a glance.

Analyst reviewing a sample in a pharmaceutical lab
Your people already know the questions. Xura gives them the answers.
One source of truth

Every system, joined into one knowledge graph.

Xura connects your MES, LIMS, QMS, and ERP and works out how a batch, a test result, a deviation, and a purchase order all relate — so a question that used to span five exports is answered in one place.

No pipelines to build, no schema to map. Point it at the systems you already run.

What Xura does

Ask the question. Xura runs the workflow.

Plain-language questions your team already asks — answered against live data, ending in the exact next actions.

Why did yield drop on the last three batches of Product X?

Batch yield & deviation analysis

Xura joins MES batch records with LIMS results and logged deviations, isolates what changed across the runs, and ranks the likely root causes with the parameters to check.

// pulls · correlates · flags CAPAs to open
Which batches are pending QC release, and what's blocking each?

QC release status

A live view of every batch awaiting release, the pending test or review holding it, and the owner — so the bottleneck is visible before it delays a shipment.

// nudges owners · escalates holds
Are we audit-ready? Show open deviations and overdue CAPAs.

Regulatory & audit readiness

Xura compiles open deviations, overdue CAPAs, and pending change controls from the QMS into one inspection-ready view, and drafts the follow-ups to close the gaps.

// assembles · assigns · tracks to close
Which starting materials fall short of the next 60 days of production?

Supply & procurement planning

It reads the production plan against current inventory and lead times, flags the key raw materials that will run short, and drafts the purchase requisitions to send.

// forecasts · drafts POs · alerts buyers
Which export orders are at risk of missing their ship date?

Order & shipment risk

Xura ties open orders to batch availability and QC status, surfaces the ones trending late, and queues the customer updates and internal escalations.

// links orders · release · logistics
Trend impurity levels for Product X across this year's batches.

Quality trending

Continuous trend analysis across batches and time, so a drift in an impurity or assay is caught early — with the affected batches and the trend line ready to review.

// trends · alerts on drift
Illustrative scenario

A specialty API manufacturer cuts a three-day yield investigation to an afternoon.

A production lead notices yield slipping on a key API. Instead of exporting batch sheets and lab results to reconcile by hand, they ask Xura. It correlates the last runs across MES and LIMS, points to a raw-material lot and a temperature deviation as the shared factors, and drafts the deviation and CAPA for QA to review — before the next batch is charged.

3 days → hours
to root-cause a yield deviation
1 knowledge graph
across MES, LIMS, QMS & ERP
Every answer
ends in the next action, ready to run

// Illustrative scenario and representative figures, shown to convey the workflow — not tied to a named customer.

Quality technician handling sample vials
From "which batches are held?" to the release, in one thread.
Answer to action

It doesn't stop at the answer.

Every response ends in the exact next moves — draft the deviation, nudge the QC owner, raise the purchase requisition, update the customer — ready for your team to approve, or set to run automatically.

The work that used to sit between the report and the result just gets done.

Built for regulated work

Your data never leaves your infrastructure.

Deploys in your environment Audit trail on every action Role-based access & approvals Human approve-to-run control Xura stores only what it learns
Xura

Put Xura to work on your plant's data.

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