GoVal Paperless Validation Solution | Stay Compliant, Stay Ahead
[ EXPERT PAPERLESS VALIDATION FOR PHARMA ]

GoVal Paperless Validation Solution.
Stay Compliant,
Stay Ahead.

GoVal was founded on the principle that validation should be efficient, compliant, and accessible. Our platform is engineered for significant validation cost reduction, replacing expensive, paper-based systems with streamlined digital workflows. We revolutionize life sciences validation with a robust GxP Compliance Software suite designed for 21 CFR Part 11 and Annex 11, ensuring audit-ready documentation and data integrity from start to finish.

With a team of validation and technology experts, we developed a robust GxP Compliance Software suite designed for 21 CFR Part 11 compliance and Annex 11 validation, delivering comprehensive pharmaceutical validation software. Our modular platform adapts to your workflow, ensuring seamless integration and scalable validation across all your systems. Experience faster audits and fewer errors with built-in best practices and real-time reporting. Our Risk-Based CSV methodology and VLMS software ensure audit-ready documentation and data integrity from requirements through execution.

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GoVal Digital Validation Platform - Pharma & Life Sciences Solutions

[ KEY BENEFITS AT A GLANCE ]

Key Features of Our GAMP 5 Validation Software.

Why Choose Our Digital Validation Platform Over Paper-Based Methods?

As the best validation platform for life sciences, GoVal's digital system revolutionizes your entire process with a secure, paperless approach. Our clients achieve rapid GxP compliance through fully automated workflows and real-time, audit-ready data trails, ensuring both efficiency and
robust data integrity.

Accelerated GxP Compliance Software

Automated workflows and real-time audit trails ensure fast and reliable compliance with regulatory standards.

100% Paperless Validation Solutions

Eliminate manual processes and reduce errors with complete digital transformation of your validation workflows.

Enhanced Audit Readiness

Our Risk-Based CSV workflows and validation automation platform automate audit trails and reports, enabling enterprise validation platform capabilities.

Continuous Validation

Integrate validation into your CI/CD pipeline. GoVal supports DevOps agility with automated regression testing and scheduled periodic reviews, ensuring a constant state of control.

Validation Workflow Automation

Automate document routing, reviews, and e-signatures. Our platform enforces 21 CFR Part 11 compliant workflows, reducing manual handoffs and accelerating validation cycles.

Hybrid Validation Deployment

Blend traditional CSV rigor with modern CSA flexibility. Our risk-based platform lets you apply the right validation strategy for each system, optimizing effort while guaranteeing GxP compliance.

Secure Data Integrity in Validation Lifecycle Management

Cloud-based platform with robust data management and security protocols ensuring data integrity.

CFR Part 11 & Annex 11 Compliance

Built on GAMP 5 validation software principles for risk-based approach. Built-in tools for regulatory adherence and global compliance standards across all regions.

Productivity Improvement with our VLMS software

Optimize workflows and enhance efficiency across your validation processes with intelligent automation.

GoVal AI - Take the Advantage of AI power

Experience the next generation of validation with Artificial Intelligence (AI) driving efficiency, accuracy, and compliance.

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Ready to Transform Your Validation Process?

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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