About
Built by pharmaceutical manufacturers.
Qualiva exists to make GMP compliance easier — not more bureaucratic. It was created by people with deep roots in pharmaceutical manufacturing and GMP, who lived the Excel deviation logs, the frantic pre-inspection SOP hunts, and the expensive consultants who weren't there at 3am.
Every feature in Qualiva traces back to a real problem in a real factory. We didn't build what we imagined pharma needed — we built what we knew it needed: a quality system that guides, rather than just stores; that gives one verified answer to "are we inspection-ready?"; and that speaks Arabic as a first language, not a translation.
Compliance software has historically been built for large Western manufacturers — heavy, English-only, and priced beyond the reach of the factories that need it most. Qualiva is built the other way around: AI-native, bilingual, and made for manufacturers across MENA and the wider world who have been underserved by both global enterprise software and generic local tools.
Our approach
What makes Qualiva different.
Guidance, not just storage
Qualiva doesn't only hold your records — it interprets deviations, drafts documents, surfaces risks, and prepares your audit responses. AI is the platform, not a feature bolted onto it.
One verified verdict
A single readiness verdict, computed by deterministic logic and traceable to your own documents — one number you can defend to an inspector, not five dashboards that disagree.
Bilingual by design
Arabic and English throughout — RTL layout, Arabic UI, Arabic document generation. Built for Arabic-speaking operations from day one, not translated for them afterwards.
The company
QUALIVA LTD — United Kingdom.
A UK-registered company (Companies House), bringing international-standard software infrastructure to pharmaceutical manufacturers. Data is hosted in the EU — Hetzner Cloud, Nuremberg, Germany — and never used for AI training.
See it running on your factory.
Request access and we'll set up your quality system — guided from day one.
Request access