ZANUS AI FOR PHARMA & BIOTECH — AUTOMATIONS

The lab’s repetitive work, set once.

Describe the job in plain words — “when a supplier COA arrives, file it to the material record and flag any out-of-trend value” — and it becomes connected blocks on a canvas, running on its own, with every run visible and retryable.

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Private tenant or your own server · unlimited users · GxP-conscious architecture

Visual automation flow with trigger, sources and actions

A real flow: inbox trigger, record sources, AI compile, three outputs — drawn from a plain description.

What it does

Deviation intake to CAPA draft

A deviation is logged; the flow pulls the batch record and SOP, drafts the narrative and a proposed CAPA, and queues both for QA — the clock starts working for you.

COAs that file themselves

Incoming certificates of analysis routed to the right material record, values extracted, out-of-trend results flagged for the quality team — no inbox archaeology.

Periodic reports on rails

The monthly stability summary, the quarterly deviation trend report, the annual product review skeleton: compiled on schedule, filed to Output, on time every time.

In a GxP shop, silent failure is not an option

Run states live on the flow: green success, red failure on the exact block that broke. A missed COA or an unfiled deviation narrative is visible the moment it happens — with a one-click retry and a run log the auditor can read.

Run log per automation, every execution recorded
One-click retry on the failed block
Finished documents in Output, statused for review

Failure state visible on the automation canvas

Life-science software is sold per validated seat and per module — a LIMS here, an eTMF there, a QMS somewhere else — while regulatory affairs still re-types the same deviation data into three systems and the literature pile grows over the weekend. Zanus AI: one AI operating system across the trial, the lab and the submission — unlimited users, GxP-conscious by architecture, hosted in your private tenant or air-gapped inside your facility.

Questions, answered

Who approves what an automation sends or files?

Your rules: queue everything for human approval, or auto-run only the steps your quality unit designates as safe. Approval gates are blocks on the canvas — visible, not buried.

The lab’s repetitive work, set once.

What it does

In a GxP shop, silent failure is not an option

Questions, answered

See it working on YOUR lab — the demo IS the product.