For regulators
One schema. An audit trail. The gaps made visible.
Thousands of clinical AI studies, pilots and deployments in one controlled vocabulary, with each product's regulatory status and an audit trail of every change we make.
For regulators
Audit trail
Every stage change and every signature is logged. The journey of each record is reconstructable.
Regulatory classification
EU AI Act risk tier, device class, and FDA and CE status are recorded per product; autonomy level on every record. Where a fact is not established the field is empty, not guessed.
What is missing, visibly
Country and patient population are on every record. Subgroup performance and oversight arrangements mostly are not, because sources rarely state them. The Library shows that gap rather than hiding it.
How AIH Lab works for regulators
AIH Lab is not a regulator. It is the infrastructure that hospitals can use to make supervision tractable: a single schema, a documented review pipeline, and an explicit audit log.
The public API and the regulator export — CSV for spreadsheets, JSON for systems, stable field semantics — cover the 25 sample records without an account. For the full catalogue, talk to us.
Start here
Regulator export
Download the 25-record public sample (JSON).
OpenSee 25 sample records
Open to everyone — chosen for spread, including thin ones.
OpenAsk for an account
Free, by invitation, and the whole Library is yours to search. Tell us who you are.
OpenAsk for a demo
After a short call, a session prepared around what you actually run.
Open