Are you ready for UDI?

Achieve regulatory compliance, reduce recalls and improve patient safety in Life Sciences

In an effort to improve the quality of information in medical device adverse event reporting, reduce recalls and improve patient safety, the United States Congress passed legislation directing the FDA to develop regulations establishing the unique device identification (UDI) system for medical devices.

Download the White paper and discover how Dassault Systèmes delivers a Global Enterprise integrated UDI system solution.

Join the discussion in our LinkedIn Group UDI & Patient Engagement