GoVal was founded on the principle that validation should be efficient, compliant, and accessible. As a leading Digital Validation Platform, we replace manual processes with automated CSV workflows. We recognized the challenges faced by life science companies relying on outdated, paper-based systems. Our Paperless Validation Solutions eliminate paper and streamline GxP compliance.
With a team of validation and technology experts, we developed a robust GxP Compliance Software suite designed for CFR Part 11 and Annex 11 validation. Our Risk-Based CSV methodology and VLMS software ensure audit-ready documentation and data integrity from requirements through execution.
[ KEY BENEFITS AT A GLANCE ]
GoVal's digital validation system revolutionizes life science validation with a secure, paperless approach. Achieve rapid GxP compliance through automated workflows and
real-time audit trails.
Automated workflows and real-time audit trails ensure fast and reliable compliance with regulatory standards.
Eliminate manual processes and reduce errors with complete digital transformation of your validation workflows.
Our Risk-Based CSV workflows automate audit trails and reports. System-generated reports and real-time data access for seamless audits and regulatory inspections.
Cloud-based platform with robust data management and security protocols ensuring data integrity.
Built on GAMP 5 validation software principles for risk-based approach. Built-in tools for regulatory adherence and global compliance standards across all regions.
Optimize workflows and enhance efficiency across your validation processes with intelligent automation.
Experience the next generation of validation with Artificial Intelligence (AI) driving efficiency, accuracy, and compliance.
Join leading pharma and other life sciences companies that rely on GoVal for digital validation—paperless VLMS, EDC, and Part 11/Annex 11–ready workflows that keep you audit-ready.
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