top of page

ERDERA: European Rare Diseases Research Alliance

Jan 24, 2025

First Edition of ERDERA Newsletter

Welcome to the First Edition of the ERDERA Newsletter!

 

We welcome 2025 and the groundbreaking opportunities it will surely bring in rare disease research. In this inaugural newsletter, we want to highlight the latest developments and initiatives from ERDERA.

Following the successful launch of our initiative in late 2024, which attracted over 600 attendees, the new year brings along calls such as ERDERA’s 2025 Joint Transnational Call and events like the RE(ACT) Congress and IRDiRC Conference, taking place from March 5-7 in Brussels. You can find out more about these initiatives below.

We are delighted to have you join us on this transformative journey to reshape the landscape of rare disease research and innovation. Together, we are building a brighter future for the 30+ million people living with a rare disease in Europe.

 

Thank you for being part of this vital community. We hope you enjoy this first edition and look forward to sharing more exciting updates in the future!



Contact us for more information!

Thanks for submitting!

Volg ons voor meer updates!

  • Linkedin
  • Instagram
  • Wix Twitter page
  • Youtube
ERN logo en tekst.png
EU logo.png
Erasmus MC logo.png

ERN CRANIO wordt gefinancierd door de Europese Unie. De inhoud van deze website vertegenwoordigt alleen de mening van de auteur en is zijn/haar enige verantwoordelijkheid. Het kan niet worden beschouwd als weerspiegeling van de standpunten van de Europese Commissie en/of het Health and Digital Executive Agency (HaDEA) of enig ander orgaan van de Europese Unie. De Europese Commissie en het agentschap aanvaarden geen enkele verantwoordelijkheid voor het gebruik dat van de informatie op deze website kan worden gemaakt.

© 2035 by San Alora

Powered and secured by Wix

bottom of page