EU AI Act Monitor
Vendor exposure analysis for high-risk AI systems, transparency filings, and procurement readiness.
4
curated source records reviewed
3
vendors with material changes
1
high-severity changes
Executive summary
What changed
This edition reviews 4 manually curated public source records across 3 healthcare AI vendors. These records are not machine-detected changes or permanent compliance claims.
1 changes are marked high severity because they affect certifications, regulatory filings, subprocessors, incidents, or material disclosure language.
The most frequently represented framework in this edition is EU AI Act. Buyers should review the source evidence and applicability to their own deployment before making a procurement decision.
Key findings
Vendor change register
Observed evidence
Ordered by latest observed date
| Observed | Vendor | Change | Framework | Severity | Source |
|---|---|---|---|---|---|
| Jun 10, 2026 | Nabla | EU AI Act Filing Published | EU AI Act | high | EU transparency filing |
| May 28, 2026 | Viz.ai | EU MDR Language Modified | EU AI Act | medium | regulatory page diff |
| May 26, 2026 | Hyro | UK GDPR Addendum Posted | UK GDPR | medium | data processing addendum |
| Apr 20, 2026 | Nabla | GDPR DPA Revised | GDPR | medium | data processing addendum |
Regulatory developments
Sources and methodology
GovernAtlas V1 uses a curated local dataset of public vendor pages, trust centers, security documentation, announcements, certification references, and regulatory disclosures. Observations indicate that public language changed; they do not independently certify legal compliance.