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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
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RD Virtual Platform
ERN consented forms
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13th European Conference on Rare Disease and Orphan Drugs
November 25, 2025
The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led policy-shaping event on rare diseases in Europe.
Clinical Research
ERDERA
Expertise Services
Funding
International Alignment
Patient Involvement (PPIE)
High-Level Meeting on a European Research and Innovation Ecosystem for Rare Diseases
November 25, 2025
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.
Accelerator
Clinical Research
Funding
International Alignment
Patient Involvement (PPIE)
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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