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About
About ERDERA
Rare Disease Dashboard
Beneficiaries and Participants
Structure and Governance
Who we are
Privacy Policy
Living with rare
Research Services
Funding
Clinical Research Network
Data Hub
Expertise services
Erdera accelerator
Training and education
International Alignment
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RD Virtual Platform
ERN consented forms
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Accelerator
Category: Accelerator
Triplet repeat expansion project sets benchmark for public-private collaboration
September 24, 2025
Accelerator
Clinical Research
Data Hub
Multi stakeholder workshop advances prioritisation of rare diseases for ATMP development
September 17, 2025
A practical framework in the making
Accelerator
Clinical Research
Data Hub
Expertise Services
Patient Involvement (PPIE)
Exploring consultancy needs for rare disease research
July 22, 2025
Mapping needs leads to tailored solutions
Accelerator
Expertise Services
“The notion that public-private collaboration is inherently problematic doesn’t align with current realities. Not only is it possible—it is necessary, beneficial, and more straightforward than many assume.”
July 7, 2025
Accelerator
Expertise Services
New toolkit strengthens collaboration between ERNs and industry
July 3, 2025
Accelerator
Clinical Research
Triplet repeat expansion project sets benchmark for public-private collaboration
June 11, 2025
Accelerator
Clinical Research
Expertise Services
World Health Assembly adopts first-ever resolution on rare diseases, signalling a new era of global collaboration
May 26, 2025
Accelerator
Expertise Services
International Alignment
Patient Involvement (PPIE)
Rare disease experts to gather in Warsaw to shape Europe’s future strategy
March 27, 2025
Accelerator
ERDERA at the Chan Zuckerberg Initiative workshop on systematically characterising rare diseases
March 27, 2025
Accelerator
Data Hub
Irene Norstedt: “The EU supports collaboration because no country alone, and no stakeholder alone, has the answer for such huge unmet needs in rare disease research”
March 11, 2025
Accelerator
International Alignment
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About
About ERDERA
Rare Disease Dashboard
Beneficiaries and Participants
Structure and Governance
Who we are
Privacy Policy
Living with rare
Research Services
Funding
Clinical Research Network
Data Hub
Expertise services
Erdera accelerator
Training and education
International Alignment
News & Updates
Resources
RD Virtual Platform
ERN consented forms
Contact Us