Eventt AI automates the testing and documentation that keeps pharmaceutical software compliant — turning weeks of manual validation into hours of auditable, regulator-ready output.
Eventt AI
What We're Building
Every pharma quality team drowns in the same documentary regime. We're building the AI-native system that treats validation artifacts as what they are — controlled documents with lifecycles — and automates the work around them.
AI reads your requirements, generates test scripts with full traceability, executes them against live systems, and captures regulator-grade evidence at every step — automatically.
A purpose-built repository for validation artifacts — with lifecycle workflows, versioning, electronic signatures, retention policies, and an immutable audit trail.
Draft Validation Plans, Summary Reports, SOPs, and more — inside the platform, with AI assistance, from structured templates and real platform context.
GxP Compliance
The auditor never asks "did your software work?" They ask for the document that proves it — with signatures from the people who attest to it.
Every action produces an audit trail. Immutable, cryptographically verifiable, and tied to the human or system that performed it. Every document goes through a controlled lifecycle — drafted, reviewed, approved with compliant electronic signatures, and archived.
Compliance isn't a bolt-on. It's the architectural foundation. The platform was designed from day one so that validation artifacts are generated as a byproduct of doing the work — not as paperwork after the fact.
Early Access
We're onboarding design partners now. Join the waitlist to get early access and shape the product with us.
No spam. We'll reach out when it's your turn.