Advancing prevention, diagnosis and treatment research for the 30 million people living with a rare disease in Europe.

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Connected for impact:

2nd International Conference on Clinical Research Networks

9 & 10 December 2025 More Info

ERDERA Funding

The 2026 Joint Transnational Call
Pre-Announcement is now live!

LATEST

News & Updates

Underrepresented countries help shape ERDERA’s roadmap for a more inclusive European rare disease research ecosystem

Successful online workshop connects underrepresented European countries in rare disease research

A landmark gathering brings together regional leaders in human genetics to reshape genomic medicine

From 9 to 11 October in Bled, the 15th Balkan Congress and 3rd Alpe Adria Meeting put rare disease diagnostics and predictive genomics centre stage.

From Vision to Reality: 6 Years of RDCA-DAP – Driving Drug Development Solutions and Innovations in Data Sharing

Presenting key achievements of RDCA-DAP in building a multi-disease rare disease database.

EU consultation on disability rights seeks evidence to strengthen inclusive research and data ecosystems

Inviting views on how a stronger EU disability strategy up to 2030 can support inclusive research, data sharing and innovation.

ERDERA

Research Services

our mission

Goals & Impacts

Unify knowledge, resources and expertise

ERDERA brings under one roof a broad range of high-value services, resources and cross-disciplinary expertise to support rare disease research projects across Europe, from planning and design to efficient execution.

Boost clinical research with and for patients

Enabling every consenting patient living with a rare disease to be findable and enrolled in a suitable clinical study that matches their needs and preferences is a core goal in ERDERA. Empowered patients can contribute to the generation of high-quality evidence to improve diagnosis, understanding of diseases and develop treatments.

Spur innovation and EU competitiveness

The new partnership aims to make Europe a global leader in rare disease research by increasing investment to spur innovation, aligning regional, national and European research strategies, and fostering collaboration among all stakeholders at global scale.

Upcoming Events

Dec
09
- 10
Dec
Tuesday,
All day
hybrid

ERDERA – the European Rare Diseases Research Alliance – is pleased to announce the upcoming 2nd International Conference on Clinical Research Networks (CRNs) for Rare Diseases, co-organised in collaboration with […]

Dec
09
- 11
Dec
Tuesday,
8:00 am - 5:00 pm
hybrid

Gathering key stakeholders, including EU policymakers, industry leaders, patient advocacy groups, researchers, and healthcare providers. Its goal is to identify concrete actions and incentives to enhance innovation across the rare disease ecosystem.

Dec
11
Thursday,
06:00 pm-07:30 pm
online

Presenting key achievements of RDCA-DAP in building a multi-disease rare disease database.

Dec
16
Tuesday,
03:00 pm-05:00 pm
onsite

This information webinar on the 2026 Joint Transnational Call for Proposals is scheduled for 16 December 2025, 15:00–17:00 CET, focusing on resolving unsolved rare genetic and non‑genetic diseases.

NEWSLETTER

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