The European Commission has just published a special ERN booklet to promote European Reference Networks. This document provides an overview of the 24 networks and showcase their achievements into the rare diseases field.
For its writing, each ERN was asked to share three success stories to show how our networks concretly and conclusively impact patient care.
The overall outlook emerging from reading this booklet is the clear EU-added value that we
provide to help patients with rare diseases and their families and the effort that the Commission is making to increase the awareness of the European Reference Networks’ activities.
You can read the booklet HERE