Valiqa (va-LEE-kah): from "validation" + "QA." Arabic for trustworthy, reliable, worthy of trust. That name is a promise to every quality engineer who has to sign their name on a validation package.
Valiqa was built by a manufacturing automation engineer with hands-on experience in PLC and HMI programming, machine vision inspection, and full IQ/OQ/PQ validation under ISO 13485 quality management systems. The work involved designing and commissioning production lines from scratch. Lines running at scale in regulated environments where documentation failures have consequences.
The validation paperwork was done manually. Every IQ protocol was a Word document assembled from a prior version. Every OQ had the same regulatory citations copy-pasted from the last one. Every PQ report started as an empty table in Excel. Meanwhile, the equipment was waiting, the line was waiting, and someone had to sit there and write it all out again.
That experience is the entire reason Valiqa exists. Not frustration with the regulatory requirements. Those exist for good reason. The frustration was with the tooling. There was no reason a skilled validation engineer should spend the majority of their time formatting documents instead of evaluating equipment.
Replace the Word/Excel/SharePoint chaos with AI-powered validation automation. Generate the documentation so teams can focus on the validation itself.
The goal is not to produce paperwork faster. It is to produce documentation that is actually correct. Proper regulatory traceability. Realistic acceptance criteria. Test steps that reflect what GHTF guidance and FDA practice actually require. When a quality engineer reviews the output, they should be reviewing substance, not correcting formatting.
Every validation document Valiqa generates must be something a qualified engineer could sign. That constraint drives every product decision.
Generate your first audit-ready validation protocol in minutes.
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