Cardiac Devices,
What Happens When the Data Starts Talking Back
After eighteen years of recording what happened, a national cardiac device registry starts revealing what will happen next.
Real-World Evidence
Patient Safety
When a device needs to be found
When a manufacturer issues a Field Safety Notice, the question is simple: which patients have this device? Patient safety depends on infrastructure, not just intention.
Cardiac Devices
Ireland joins the European story on dual-chamber leadless pacing
Ireland's first dual-chamber leadless pacemaker system was completed at the Mater Misericordiae University Hospital and captured on HRI's national cardiac device registry in real time. Here is why that matters for the future of cardiac device evidence.
Health Data
Trust Is Not a Contract
The UK Biobank breach is a 500,000-person case study in the difference between a contract and an architecture, and a warning for how the European Health Data Space gets built