AXIOM · Healthcare

AI Governance.
Before it reaches your systems.

AXIOM sits between your AI and your clinical systems. Every output validated, audited, and logged before it arrives, under HIPAA, EU AI Act, 42 CFR Part 2, and GxP. No bypass. Zero Trust at runtime.

The regulator is coming. Can you prove what your AI produced?

HIPAA doesn't have an AI exception. Neither does the FDA. The EU AI Act classifies clinical decision support as high-risk, with mandatory audit trails, human oversight documentation, and conformity records.

When an auditor walks through your door, you need to prove what generated every AI output, who reviewed it, and whether it was compliant at the moment it was used.

One API. Three steps. Every output covered.

Step 01, You plug in. One API call routes your AI outputs through AXIOM before they reach your EHR, clinical workflow, or pharma data environment. No rebuild. No downtime.

Step 02, We enforce. Every output validated against HIPAA, EU AI Act, 21 CFR Part 11, 42 CFR Part 2, GxP. PHI masked. Consent enforced. Non-compliant outputs held and escalated.

Step 03, You're covered. Every output cryptographically signed and logged. When a regulator asks for proof, you open the dashboard.