Built by pharmaceutical manufacturers,
for pharmaceutical manufacturers.

Qualiva was born from a simple frustration: the tools that pharmaceutical QA teams actually need didn't exist.

Our Story

We built the tool we always wished we had.

Qualiva was created by a team with deep roots in pharmaceutical manufacturing across the MENA region. After years of working inside factories β€” experiencing firsthand the knowledge gaps, the Excel-based deviation logs, the frantic SOP searches before inspections, the expensive consultants who weren't available when you needed them β€” we decided to build the tool we always wished we had.

Every module in Qualiva exists because a real factory needed it. Not because a product manager read a market report. The Issue Troubleshooter was built because junior QA staff needed a reliable guide to root cause analysis. The Stability Studies module was built because climate zone IVb support was simply missing from every Western QMS. The Ask Qualiva AI assistant was built because no one should face a 3am production crisis alone.

QUALIVA LTD is a United Kingdom registered company, bringing international-standard software infrastructure to pharmaceutical manufacturers who have been underserved by both global enterprise software and generic local solutions.

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Built inside factories

Every feature traces back to a real problem in a real factory. We didn't build what we thought pharma needed β€” we built what we knew it needed.

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Arabic-first by design

Not an afterthought. The platform was designed from day one for Arabic-speaking operations β€” RTL layout, Arabic UI, Arabic document generation.

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UK registered entity

QUALIVA LTD β€” Companies House, United Kingdom. International legal and contractual standards for every customer.

Turn every pharmaceutical factory in the Arab world into a GMP-compliant, audit-ready, knowledge-driven operation β€” without consultants, without complexity, without compromise.

Why Qualiva is different.

Three things that no other GMP platform offers together.

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AI-native

Every module is intelligently assisted. Qualiva analyses deviations, suggests root causes, drafts documents, flags risks, and prepares audit responses. AI is not a feature. It is the platform.

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Arabic-first

Fully bilingual β€” Arabic and English throughout. RTL layout, Arabic UI, Arabic document generation, Arabic voice input. Built for the region, not translated for it.

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Pharma insiders

Built by a team with deep pharmaceutical manufacturing expertise across MENA. Every feature exists because a real factory needed it.

Regulatory coverage.

WHO GMP (TRS 986, TRS 1044)
EU GMP Parts I & II
Annex 11
Annex 1
ICH Q9
ICH Q10
ICH Q1A–Q1F
Arab GMP Code
SFDA (Saudi)
EDA (Egypt)
Climate Zone IVb

Company information.

Company nameQUALIVA LTD
RegistrationCompanies House, United Kingdom
AddressLondon, United Kingdom
Contacthello@qualiva.ai
Data infrastructureHetzner Cloud, Nuremberg, Germany
Founded2025

See what Qualiva can do for your factory.

One 45-minute demonstration. No sales pitch. A working demo with your factory's real GMP challenges.

Request a Demo See our modules β†’
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