Purpose-Built for GxP

VEEVA CERTIFIED

AI-Powered Validation Automation for Veeva Vault

End-to-end validation for GxP environments. Built to accelerate validation outcomes — automated test creation, parallel execution, evidence generation, and audit-ready reporting. Certified by Veeva. Trusted by 8 of the top 10 global pharma.

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15-minute personalized walkthrough. No setup required.

80%

Faster validation cycles V-Assure production deployments

50+

Deployments worldwide Active validation engagements

Top 10

Pharma trusted Top 10 global pharma references

Manual Validation Is Holding Your Team Back

Weeks of Manual Scripting

Writing test scripts by hand for every Vault configuration change creates bottlenecks and delays releases. Your validation team is spending 40% of time on manual paperwork.

Evidence Assembly Nightmares

Gathering screenshots, logs, and approvals across systems for audit packages takes days of tedious work. Incomplete evidence put inspections at risk or requires rework.

Regulatory Risk from Human Error

Manual processes introduce inconsistencies. One missed step can trigger audit findings and compliance gaps. Your liability increases with each manual validation cycle.

From Configuration to Compliance in Four Steps

V-Assure automates the entire validation lifecycle, from requirement discovery to audit-ready reporting.

Discover

V-Assure automatically scans your Vault configuration, identifying validation-relevant changes and mapping test requirements to your business processes. No manual discovery needed.

Generate

AI creates comprehensive test scripts tailored to your specific Vault setup — IQ, OQ, PQ protocols aligned to your validation plan. Each script includes expected results and evidence checkpoints.

Execute

Parallel test execution across environments with real-time monitoring. Automated evidence capture at every step — screenshots, system responses, timestamps, and user actions all recorded automatically.

Report

Audit-ready validation packages generated automatically. Full traceability from requirement to evidence, organized for QA review and approval. Ready for FDA inspection.

Built for Validation Teams, Certified by Veeva

Six core capabilities that transform how you validate Veeva Vault.

Automated Test Scripts

AI Creates Complete Test Suites in Minutes

V-Assure analyzes your Vault configuration and generates comprehensive IQ/OQ/PQ test scripts. Every test is automatically tailored to your specific setup with expected results and compliance requirements baked in.

Real-Time Monitoring

Watch Parallel Execution Across Environments

Execute tests simultaneously across dev, UAT, and production environments. Real-time progress bars, live status indicators, and instant failure alerts keep your team informed every step of the way.

Audit-Ready Reports

Export Complete Validation Packages in One Click

Generate FDA 21 CFR Part 11 compliant validation packages with full traceability from requirements to evidence. All screenshots, timestamps, approvals, and system responses automatically compiled and organized for regulatory submission.

Automated Test Script Generation

AI analyzes Vault configurations and generates complete IQ/OQ/PQ test scripts. No manual scripting required. Every script includes expected results and pass/fail criteria.

Parallel Test Execution

Run tests across multiple environments simultaneously, reducing cycle time from weeks to days. Real-time progress monitoring and instant failure alerts keep your team in control.

Evidence Auto-Capture

Every test step automatically captures screenshots, timestamps, and system responses as audit evidence. No manual evidence gathering. Complete traceability from test to proof.

GxP-Aligned Reporting

Pre-formatted validation reports that meet FDA 21 CFR Part 11, EU Annex 11, and GAMP 5 requirements. Organized for QA review and regulatory submission.

Change Impact Analysis

Instantly understand which tests need re-execution when configurations change. No more guesswork. Regulatory-compliant impact assessment built in.

Continuous Validation

Shift from periodic to continuous validation. Monitor compliance posture in real-time across your Vault landscape. Proactive risk detection before issues reach production.

Veeva Certified. Enterprise Proven.

V-Assure is certified by Veeva for Vault Quality, Vault RIM, Vault Clinical, and Vault Safety. Your compliance team can verify certification in the Veeva Partner Marketplace today.

Certified for:

Vault Quality (validated for QMS workflows)
Vault RIM (regulatory intelligence & maintenance)
Vault Clinical (clinical trial management)
Vault Safety (pharmacovigilance systems)
Built on Veeva Vault APIs (no custom integrations)
Native Vault UI integration (no training required)
SSO & role-based access control
SOC 2 Type II compliant

Measurable Impact on Validation Operations

80%

Reduction in validation cycle time

Less manual effort per release

Zero

Audit findings from V-Assure validations

<48h

Config change to validated state

Customer Success

V-Assure transformed our validation approach. What used to take our team six weeks per major release now takes less than a week. The audit packages are more thorough than anything we produced manually, and our regulatory team has never been more confident in our validation evidence.

Ready to Automate Your Validation?

See how V-Assure can reduce your validation cycles by 80% while strengthening compliance. Veeva-certified. Audit-ready. Production-proven.

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Veeva Certified

SOC 2 Type II

ISO 27001

GxP Compliant

FDA 21 CFR Part 11