EURORDIS - RARE DISEASES EUROPE
- Country
- France
- Type
- Beneficiary
- Website
- www.eurordis.org
- Grants received
- 23
Funding record
- 23 grants on record
- €8,490,791.11 awarded in total
- 2012–2025 span of the record
Grants recorded here are the ones our sources publish, and the total is the sum of those. It is not a statement of this organisation's total funding.
Programmes
11 further grants are on record without a programme named by the source, or under a programme outside the largest shown here.
Frequent partners
Organisations this one has been funded alongside on two or more projects. A single shared consortium is not counted: the largest here has 195 members, and being on one list together is not a collaboration.
- INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
- ACADEMISCH ZIEKENHUIS GRONINGEN
- ASSISTANCE PUBLIQUE HOPITAUX DE PARIS
- ASTRAZENECA AB
- CHARITE - UNIVERSITAETSMEDIZIN BERLIN
- ISTITUTO SUPERIORE DI SANITA
- UPPSALA UNIVERSITET
- BAYER AKTIENGESELLSCHAFT
Calls from this organisation
No published calls from this organisation.
Grants received
- PUBLIC ENGAGEMENT IN RESEARCH INFRASTRUCTURES FOR MISSION CANCER: MANAGING COMPLEXITY OF EMERGING TECHNOLOGIES
- Comprehensive methodological and operational approach to clinical trials in rare and ultra-rare diseases
- EUROPEAN RARE DISEASES RESEARCH ALLIANCE
- MAP, JOIN AND DRIVE EUROPEAN ACTIVITIES FOR ADVANCED THERAPY MEDICINAL PRODUCT DEVELOPMENT AND IMPLEMENTATION FOR PATIENT AND SOCIETY BENEFIT
- Medicine Made to Measure.
- More Effectively Using Registries to suppOrt PAtient-centered Regulatory and HTA decision-making
- BUILDING A SUSTAINABLE EUROPEAN INNOVATION PLATFORM TO ENHANCE THE REPURPOSING OF MEDICINES FOR ALL
- FrAmework for ClInicaL trIal participants daTA reutilization for a fully Transparent and Ethical ecosystem
- Shortening the path to rare disease diagnosis by using newborn genetic screening and digital technologies
- European Rare dIsease research Coordination and support Action
- Next Generation Health Technology Assessment to support patient-centred, societally oriented, real-time decision-making on access and reimbursement for health technologies throughout Europe
- European Joint Programme on Rare Diseases
- conect4children (COllaborative Network for European Clinical Trials For Children)
- Patients Active in Research and Dialogues for an Improved Generation of Medicines: Advancing meaningful patient engagement in the life cycle of medicines for better health outcomes.
- Solving the unsolved Rare Diseases
Data source
© European Union, 2026. Source: CORDIS. Reused under Commission Decision 2011/833/EU — CC BY 4.0.
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