AI-Powered Paperless Validation
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Digitize your validation lifecycle for Pharma & Life Sciences.
GoVal VLMS replaces manual, paper-heavy validation with a modern, audit-ready, AI-assisted platform built for regulated industries. Achieve 21 CFR Part 11 & GxP compliance faster, with full traceability.
- Up to 40–60% faster validation cycles.
- End-to-end digital workflows, approvals and e-signatures.
- Real-time audit trails, version control and ALCOA+ compliance.
Built for compliance-driven teams
Aligned with global pharma regulations:
21 CFR Part 11 EU Annex 11 GAMP 5 GxP / ALCOA+
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See how GoVal VLMS can streamline your validation lifecycle & improve audit readiness.
Is GoVal compliant?
Yes — built for 21 CFR Part 11, Annex 11 & GxP.
Yes — built for 21 CFR Part 11, Annex 11 & GxP.
How fast can we start?
Most teams onboard within days.
Most teams onboard within days.