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 years covered
This total adds up only the grants our sources publish. It is not the total funding this organisation has received.
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 funded alongside this one on two or more projects. Sharing a single project does not count. Some projects have as many as 195 participants, and appearing on the same list once is not a working relationship.
- INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
- ACADEMISCH ZIEKENHUIS GRONINGEN
- UPPSALA UNIVERSITET
- ASSISTANCE PUBLIQUE HOPITAUX DE PARIS
- ASTRAZENECA AB
- CHARITE - UNIVERSITAETSMEDIZIN BERLIN
- EATRIS ERIC
- FUNDACIO PRIVADA PER A LA RECERCA I LA DOCENCIA SANT JOAN DE DEU
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.
We collected this from the source on .
Personal data of natural persons has been dissociated by quiescence.eu.
This service is not affiliated with, sponsored or endorsed by the data publishers.