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Validation 4.0
Reimagined.

Generate GAMP-driven OQ test suites in minutes. Experience the future of pharmaceutical validation with AI-powered assurance.

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The Manual CSV Nightmare

Why are you still writing tests by hand?

Traditional validation is slow, expensive, and prone to human error. It's time for Validation 4.0.

Weeks of Delay

Manual protocol writing bottlenecks project timelines. A single system can take 2-3 weeks to validate manually.

High Costs

Validation consultants cost $150+/hr. We reduce generation costs to pennies per test suite.

Compliance Risks

Manual scripts often miss requirements or lack traceability, leading to painful audit findings.

AI-Driven Computer Software Assurance (CSA)

Shift from documentation-heavy validation to critical thinking and automated assurance.

95% Faster

Generate complete, compliant OQ test suites in 8-12 minutes.

Audit Ready

Full ALCOA+ data integrity, electronic signatures (21 CFR Part 11), and immutable audit trails.

Risk-Based

Automatic GAMP 5 categorization ensures you focus testing efforts where risk is highest.

Join the Validation 4.0 revolution. Secure, compliant, and efficient.

GAMP-5 Compliant

21 CFR Part 11 Ready

ALCOA+ Validated