Pharmaceutical
LIMS, ERP, QMS, safety databases, partner portals — and between them, your people have become the integration layer. ZADS take on the re-keying without changing a validated system.
What's slowing you down
LIMS, ERP, QMS, regulatory and safety databases, distributor and partner portals — each one validated, none built to talk to the next.
Where the connections stop, people fill the gap: QA, QC and supply teams re-keying results, batch data and shipment details from one screen into the next.
GxP and 21 CFR Part 11 systems cannot be casually changed, so every new interface means change control, a new project or a new vendor.
Batch records, adverse-event cases and serialization data all have to stand up to review. Every step has to be shown, not just described.
How ZADS run it
Validated systems, worked at the screen
An AI Digital Specialist works your LIMS, ERP, QMS and partner portals at the user interface, exactly like a trained operator — no new APIs, no source-code changes to validated systems.
Your people keep the decisions
ZADS is a Human-AI Orchestration Platform: ZADS execute the repetitive coordination — batch data into the record, case intake into the safety database, shipment and serialization updates across portals — while your people keep control of decisions, approvals and exceptions. Every step is logged, an audit trail your quality team can actually review.
Proven under pressure
This technology was proven with the US military, where systems are locked down and mistakes cost more than money. It accelerates your quality, regulatory and supply teams. It never replaces them.
See what ZADS could do across your validated systems
A 15-minute walkthrough of how ZADS would bridge your LIMS, ERP, QMS and partner portals — under your governance, with every step on record.