AI-Powered Paperless Validation
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GxP compliance & GAMP 5 validation software for Pharma & Life Sciences.
GoVal VLMS is a modern, paperless GxP compliance software and GAMP 5 validation platform built for regulated teams. Digitize validation workflows, approvals, and audit evidence to stay inspection-ready 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.
Common use cases
Validation Lifecycle Management (VLMS) Risk-based CSV Paperless Validation Digital Validation Evidence
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 using GoVal VLMS?
Onboarding is typically quick, especially when your SOPs and validation templates are already organized and ready to use. GoVal aligns smoothly with your existing processes, and our team can support you during setup to help ensure a fast and efficient implementation experience.
Onboarding is typically quick, especially when your SOPs and validation templates are already organized and ready to use. GoVal aligns smoothly with your existing processes, and our team can support you during setup to help ensure a fast and efficient implementation experience.