We are a non-profit organisation recognised by the Italian Ministry of Education, Universities and Research. We were founded in 1990 in response to calls by people suffering from rare diseases.
Right from the start, we have always listened to patients, to provide the answers they need. Every day.
We manage fund raising activities and guarantee the necessary resources for our research projects. These projects are subjected to rigorous assessments on the part of an independent, international Scientific and Medical Committee.
Our Board of Directors
- Luca di Montezemolo (Chairman)
- Omero Toso (Deputy Chairman)
- Francesca Pasinelli (Director General)
- Alberto Fontana
- Luca Garavoglia
- Fabio Gallia
- Lupo Rattazzi
- Andrea Munari
- Giovanni Manfredi
- Carlo Pontecorvo
- Isabella Seràgnoli
How we fund research
Research funds are assigned throught the help of:
Scientific and Medical Committee: follows the peer-review procedure. Before the plenary discussion, each proposed project is examined by three committee members and at least two external reviewers selected from the international community. Thanks to this process, we can be sure that only the best projects are chosen.
Scientific Steering Committee: the task of the Scientific Steering Committee is to support the overall policy and management decisions of the Board of Directors within the framework of biomedical research.