SCREENGEN
Newborn screening and genetic analysis of rare diseases: development of Euro-regional infrastructure and cooperation
Perustiedot
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Lyhyt kuvaus konsulttiyrityksestäThe aim of the project is to provide health service of high technical level with equal chances for the whole population of the Euro-region, as well as medical effectiveness by developing a common infrastructure and a Euro-regional centre for metabolic and genetic selective screening. The main activities of this project are: construction of a laboratory in Szeged, renovation of two laboratories in Arad and Timisoara, acquisition of equipments and supplies, development of diagnostic methods, investigation of target group and human resources development. The target groups of the project are newborns, patients with inherited disorders (haemophilia, cystic fibrosis, Duchene disease, their families and relatives as well all the population of the three counties.
- Projektin suunniteltu aloitus 01.05.2011 Projektin odotettu loppu 31.01.2013
- Kesto 20 (kuukaudet))
Talousarvio
- Ohjelman / ehdotuspyynnön kokonaisbudjetti 1933810 Hankkeen EU-rahoitus 1640727 Prosentti: 85
kumppanit
Asiakirjat
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