Forensic Governance Infrastructure · Pharma & Life Sciences

Proven before it acts.
Reasoned before it's signed.

Every regulated institution now has to prove its AI, to a regulator, an auditor, a safety officer. In pharmacovigilance and clinical decisions, a flag isn't enough: someone has to show why. The evidence answers that: every finding your AI surfaces is grounded in a verified fact and the exact rule behind it, and signed, reasoned evidence you show the regulator to prove your pharma AI is clean.

Every finding grounded in fact, evidence, and the exact regulation.

VERUM connects to your systems via REST API and reasons over what your AI produces. Compliant outputs pass automatically, it surfaces only what needs you, and grounds every finding in a verified fact and the precise rule behind it.

For pharmacovigilance and clinical work, VERUM checks outputs against real clinical and pharmaceutical facts, diagnoses, medications, drug interactions, adverse events, contraindications, and cites the precise regulatory clause behind every finding: EU AI Act, HIPAA, 21 CFR Part 11, GxP, ALCOA+.

Every answer VERUM produces is held to the same standard it enforces: protected, grounded in the fact and the rule, signed and logged, and, where the risk requires it, approved by a named human. The reasoning that checks your AI is governed the same way.