Data and AI EU AI Act readiness

EU AI Act readiness.

  • Obligations arrive in stages.
  • Your ISO 42001 evidence maps onto them.

What it asks of AI in healthcare.

Risk management

A documented system, kept current.

Data governance

Training data you can account for.

Human oversight

Designed in, not added on.

Technical documentation

Ready for assessment.

Monitoring in use

Performance watched after release.

In the UK, the direction is the same.

In October 2026 the UK Government accepted all 44 recommendations of the National Commission into the Regulation of AI in Healthcare. Regulation is moving from one-off approval towards assurance across a product's whole life. Qyro keeps that evidence current: continual lifecycle monitoring, on one record.

Start with the management system.

ISO 42001 gives you the structure the Act expects.

See it with your own standards.