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Welcome to EJP RD

The European Joint Programme on Rare Diseases (EJP RD) is a programme aiming to create an effective rare diseases research ecosystem for progress, innovation and for the benefit of everyone with a rare disease. We support rare diseases stakeholders by funding research, bringing together data resources & tools, providing dedicated training courses, and translating high quality research into effective treatments.

Follow us on social media!

Watch Our Introduction Video

What is the European Joint Programme on Rare Diseases? How EJP RD works? What kind of support EJP RD provides? How to contact EJP RD?

Free workshops!

For personnel affiliated to institutions of the European Reference Networks

Latest News

Save the date: RE(ACT) Congress and IRDiRC Conference 2025

3 mai 2024

Welcome to the pinnacle event in rare diseases research – the RE(ACT) Congress…

Third EJP RD MOOC on “Health Data Ethics & Regulatory Frameworks in Rare Disease Research”

30 avril 2024

🚀 Our third EJP RD MOOC on “Health Data Ethics & Regulatory Frameworks…

Interim Analysis, Adaptations and Master Protocols (VIDEO)

26 avril 2024

https://youtu.be/_O8qJ5m2ytU Today we release our latest online course on “Interim Analysis, Adaptations, and…

Upcoming Events

15

Mai

2024

Save the date: 12th European Conference on Rare Diseases and Orphan Products (ECRD)

The 12th edition of the European Conference on Rare Diseases and Orphan Products (ECRD), for which EJP RD is a partner, will take place on 15-16 May 2024, both online and in Brussels! It will be held as an official event under…

  • 08:30 - 17:30 (16 mai 2024)
  • Brussels, Belgium

17

Mai

2024

Key Solutions to Model Longitudinal Natural History  Data Application in Ataxia Disease

Description will be updated soon. More information on intermediate courses and Clinical Trials Methodology Watch all the intermediate courses

  • 14:00 - 14:00
  • Youtube
35
COUNTRIES
130
INSTITUTIONS
24
ERNs
1200
SCIENTISTS AND ADMINS