WAVAmed builds AI-powered software for early detection of clinical deterioration in general ward and post-discharge patients, developed as a regulated medical device under the EU Medical Device Regulation.
Every year, 11 million people die from sepsis. It accounts for 1 in 5 deaths globally. The majority are preventable.
The failure is not in ICU treatment. The failure is in what happens before the ICU. In general wards, deteriorating patients are not continuously tracked. Warning signs are missed. By the time standard protocols raise an alarm, the window for early intervention has closed.
Existing clinical AI tools are designed for patients already in intensive care. No CE-marked AI covers the full continuum, from ward admission through 30 days post-discharge. That is the gap where patients are lost. That is what WAVAmed is built for.
What we build
Clinical evidence
The general ward is a monitoring dead zone. So is the first month after discharge. Patients deteriorate unnoticed in both. We are building the intelligence layer for both.
We are open to conversations with clinical partners, hospital systems, investors, and regulatory collaborators across Europe and MENA.