TY - GEN
T1 - The legal regulation of biobanks. National report: Italy
AU - Sándor, Judit
AU - Mauro, Christiana
AU - Bárd, Petra
PY - 2009
Y1 - 2009
N2 - As partners in the European Union Framework Project entitled “GeneBanC: Genetic bio and dataBanking: Confidentiality and protection of data” we are exploring the legal regulations of data- banks. The Center for Ethics and Law in Biomedi- cine established at the Central Euro- pean University, Budapest aimed to investigate the existing regulatory frame works of bio- banks across the EU and focus on the collection and analysis of legislation and regulation regarding the establishment, management and functioning of classical, population and forensic bio- banks across Europe. An important objective was to look at the similarities and differences in such legislation and regulations, in order to formulate recommendations towards a harmonization of European practices and regulations. The European jurisdiction was divided up into two parts between CELAB and the Belgian project partner, the Centre for Biomedical Ethics and Law, K.U.Leuven. CELAB focused on the regulatory framework of Cyprus, the Czech Republic, Estonia, Greece, Hungary, Italy, Latvia, Li huania, Malta, Poland, Romania, the Slo- vak Republic, and Slovenia. The present booklet is the first one in the series of country reports prepared by CELAB.
AB - As partners in the European Union Framework Project entitled “GeneBanC: Genetic bio and dataBanking: Confidentiality and protection of data” we are exploring the legal regulations of data- banks. The Center for Ethics and Law in Biomedi- cine established at the Central Euro- pean University, Budapest aimed to investigate the existing regulatory frame works of bio- banks across the EU and focus on the collection and analysis of legislation and regulation regarding the establishment, management and functioning of classical, population and forensic bio- banks across Europe. An important objective was to look at the similarities and differences in such legislation and regulations, in order to formulate recommendations towards a harmonization of European practices and regulations. The European jurisdiction was divided up into two parts between CELAB and the Belgian project partner, the Centre for Biomedical Ethics and Law, K.U.Leuven. CELAB focused on the regulatory framework of Cyprus, the Czech Republic, Estonia, Greece, Hungary, Italy, Latvia, Li huania, Malta, Poland, Romania, the Slo- vak Republic, and Slovenia. The present booklet is the first one in the series of country reports prepared by CELAB.
UR - https://m2.mtmt.hu/api/publication/2577791
M3 - Other contribution
SN - 9789638840486
T3 - CELAB paper series, ISSN 2074-4498 ; 10.
PB - Central European University (CEU)
CY - Budapest
ER -