Validation Lifecycle Management Software solutions built for
every GxP workflow
GoVal brings CSV, CSA, equipment qualification, paperless execution, GxP compliance, and data integrity into one modern VLMS platform — so your team can validate faster and stay inspection-ready.
Unified Validation Platform
Choose your validation priority. Connect requirements, execution, and approvals in one unified, audit-ready system.
Computer System Validation
Manage URS, risk, testing, and reporting in a single GAMP 5 aligned workflow.
Computer Software Assurance
Apply risk-based assurance with scripted, unscripted, and audit-ready GxP testing.
Equipment Qualification
Digitize qualification protocols across IQ, OQ, and PQ with real-time reporting.
Paperless Validation
Replace manual routing and physical binders with secure, digital validation.
Audit-Ready Security & Compliance
Backed by immutable audit trails, ALCOA++ integrity, and ISO 27001 certified infrastructure for continuous inspection readiness.
GxP Compliance Management
Align validation and quality teams with controlled workflows, CAPA, and change visibility.
Data Integrity & Audit Trail
Protect records with secure e-signatures, immutable audit trails, and role-based controls.
Security & Infrastructure
ISO 27001 certified security, GDPR compliance, and end-to-end controls for GxP environments.
Validation Solutions by Industry
Tailored validation workflows for life sciences organizations worldwide.
Pharmaceutical Validation
For API, OSD, sterile, and generic pharma teams.
Biotech Validation
For biologics, cell & gene therapy, and scaling biotech.
Medical Device Validation
For device software, SaMD, and IEC 62304 workflows.
CMO / CRO Validation
For isolated workspaces and client audit readiness.
Clinical Research Validation
For EDC, eTMF, CTMS, and Part 11 controls.
ROI Tools & Pricing Plans
Quantify your time savings and find the perfect plan for your validation team.
Common questions about GoVal solutions
Short answers for validation, QA, IT, and compliance teams evaluating a modern VLMS platform.
What is a Validation Lifecycle Management System (VLMS)?
A Validation Lifecycle Management System (VLMS) is a purpose-built digital platform that manages the complete GxP validation lifecycle — from User Requirements Specification (URS) and risk assessment through IQ/OQ/PQ execution, electronic approval, change control, periodic review, and Validation Summary Report generation. GoVal is a cloud-native VLMS that replaces fragmented tools like Word, Excel, and SharePoint with a single, audit-ready, 21 CFR Part 11 compliant platform.
What validation solutions does GoVal provide?
GoVal provides a unified VLMS covering: Computer System Validation (CSV), Computer Software Assurance (CSA), equipment IQ/OQ/PQ qualification, paperless validation, GxP compliance management, data integrity and ALCOA+ enforcement, and industry-specific workflows for pharmaceutical, biotech, medical device, CMO, CRO, and clinical research organisations.
What is the best validation software for pharmaceutical companies?
The best pharmaceutical validation software provides a complete, audit-ready validation lifecycle in a single platform — covering GAMP 5 risk classification, paperless IQ/OQ/PQ execution, live Requirements Traceability Matrix, 21 CFR Part 11 e-signatures, deviation tracking, and one-click Validation Summary Report generation. GoVal is purpose-built for pharma, biotech, and life sciences validation teams.
Does GoVal support 21 CFR Part 11 and EU Annex 11?
Yes. GoVal supports electronic records, electronic signatures with meaning statements, role-based access control, user attribution, timestamped tamper-evident audit trails, and controlled workflows fully aligned with 21 CFR Part 11 and EU GMP Annex 11 requirements.
How does GoVal support paperless validation?
GoVal replaces paper-based templates, manual routing, wet-ink signatures, and physical binders with controlled digital workflows, 21 CFR Part 11 e-signatures, real-time execution, automated RTM traceability, and instant Validation Summary Report generation. Most teams reduce validation cycle time by 50–60% after going live.
How long does it take to implement GoVal?
Most life sciences teams go live with GoVal in 3–6 weeks. GoVal ships pre-validated with vendor IQ/OQ documentation included, so teams operate in a compliant environment immediately — without the 6–12 month implementation timelines typical of legacy enterprise VLMS platforms.
Can GoVal be used across multiple sites?
Yes. GoVal is a multi-site, enterprise-grade platform supporting shared validation templates, controlled role-based access, centralised dashboards, and site-level execution tracking — covering everything from a single facility to a global network of manufacturing and research sites.
Is GoVal ISO 27001 certified?
Yes. GoVal is ISO 27001 and ISO 9001 certified, GDPR compliant, and built on secure cloud infrastructure designed for regulated life sciences environments — with end-to-end encryption, controlled data residency options, and regular third-party security audits.