This section is dedicated specifically to researchers. You will find here the information about the opportunities of rare diseases research funding at the national level in "National RD funding initiatives" and "Next generation sequencing facilities database" that groups sequencing platforms from Europe and Associated countires.
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“Vaincre la Mucoviscidose” is a non-profit organization created in 1965 by parents of children with CF. The foundation follows 4 goals :
- Cure CF by helping and financing research in France and all around Europe
- Treat right now by improving health care
- Improve quality of life in order to make a life with CF more acceptable and bearable
- Alert on the gravity of CF by communicating toward the public in general and towards parents and family affected with CF.
95% of VLM resources come from people’s charity and generosity.
Title of the programme: no title
Type of the programme: thematic call for proposals
The VLM Foundation funds basic and clinical research. Subventions cover the period of 1 - 3 years and allow financing of personnel (PhD students, post-doctoral fellows) and operating expenses
Recurrence of the programme: yearly
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For more information ABOUT E-Rare please contact:
E-Rare Coordinator
Daria JULKOWSKA
Tel.: +33(0) 1 78 09 80 78
+33(0) 6 20 14 13 81
daria.julkowska@agencerecherche.fr
Agence Nationale de la Recherche - ANR
Health & Biology Department
50 Avenue Daumesnil
75012 Paris, France