Advancing prevention, diagnosis and treatment research for the 30 million people living with a rare disease in Europe.
The Joint Transnational Call 2026 is
now open!
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ERDERA Survey
Exploring consultancy needs for rare disease research
LATEST
News & Updates
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 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
Help Shape the Future of Rare Disease Evidence Generation!
Join Our Upcoming Webinar: Putting Patients at the Center of Rare Disease Clinical Trials
The training responds to the growing need for patient advocates to understand data management, ethical considerations and the role of AI in rare disease research.
The two-day event will focus on translating research and policy initiatives into tangible benefits for Rare Disease patients through better prevention, diagnosis, and treatment.
Join the leading international drug repurposing conference to explore the future of patient-centric medicines repurposing!
The next ECRD will take place on 3–4 June 2026 in Prague under the title “Rare Diseases in a Changing & Competitive Europe: Shaping policies to address the unmet needs of people living with rare diseases”.
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