GoVal

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Govalidation is a web-based application that helps to perform the validation life cycle in a digital way. A configurable workflow that helps to review & approve cycle in an automated way. GoValidation is designed in compliance with 21 CFR Part 11 and regulatory requirements taking inputs from industry experts and followed the best standards. The system requires Zero paper usage and 100% electronic way of document generation.

GoVal

0 reviews

GoVal – AI-Powered Paperless Validation Software for Pharma & Life Sciences GoVal is an advanced digital validation platform designed for pharmaceutical, biotech, and life sciences companies to streamline and automate their validation processes. By replacing traditional paper-based workflows, GoVal reduces manual effort by up to 50%, significantly improving productivity, accuracy, and compliance. Built to meet stringent regulatory requirements, GoVal ensures full compliance with FDA 21 CFR Part 11, EMA, EU Annex 11, and other global regulatory guidelines, providing a robust audit trail, e-signatures, and complete data integrity. Its AI-powered features simplify risk assessments, Requirement Traceability Matrices (RTM), Validation Summary Reports (VSR), and other compliance documents—all generated automatically from project data, reducing time and human errors. GoVal delivers high ROI by minimizing validation cycle times, reducing costly rework, and enabling teams to focus on innovation rather than paperwork. Whether for computer system validation (CSV), equipment qualification, or process validation, GoVal is the go-to solution for organizations seeking faster, smarter, and fully compliant validation processes. Key Highlights: * Up to 50% reduction in manual work and validation effort. * Automated reporting (RTM, VSR, and compliance docs). * AI-enabled risk assessment and document intelligence. * Seamless regulatory compliance (FDA, EMA, WHO). * Quick ROI with faster deployment and digitized workflows.