Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Zsuza Temesvari"'
Autor:
Gabriella Kardos, Xina Grählert, Margaret Cooney, Raquel Hernandez, György Blaskó, Anke Strenge-Hesse, Mariantonia Serrano, Wolfgang Kuchinke, Timothy O'Brien, Christine Kubiak, Fernando de Andres, Arrigo Schieppati, Christian Gluud, Jacques Demotes, Jean-Marc Husson, Hanna Johansson, Diana Winter, Siobhan Gaynor, Nuria Sanz, Steffen Thirstrup, Béatrice Barraud, German Kreis, Sebastian Geismann, Kate Whitfield, Charlotte Asker-Hagelberg, Lea Stankovski, Christian Libersa, Gabriele Dreier, Adeeba Asghar, Zsuza Temesvari, Karl-Heinz Huemer
Publikováno v:
Trials
Trials, BioMed Central, 2010, 11 (1), pp.104. ⟨10.1186/1745-6215-11-104⟩
Trials, Vol 11, Iss 1, p 104 (2010)
Trials, BioMed Central, 2010, 11 (1), pp.104. ⟨10.1186/1745-6215-11-104⟩
Trials, Vol 11, Iss 1, p 104 (2010)
Background 'Compassionate use' programmes allow medicinal products that are not authorised, but are in the development process, to be made available to patients with a severe disease who have no other satisfactory treatment available to them. We soug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41797ac93026cc092a607f64abde60a0
Autor:
Jean-Marc Husson, Timothy O'Brien, Fernando de Andres, Charlotte Asker-Hagelberg, Béatrice Barraud, Nuria Sanz, Zsuza Temesvari, Karl-Heinz Huemer, Sue Bourne, Gabriele Dreier, German Kreis, Adeeba Asghar, Hanna Johansson, Jacques Demotes-Mainard, György Blaskó, Siobhan Gaynor, Xina Grählert, Arrigo Schieppati, Jane Byrne, Kate Whitfield, Gabriella Kardos, Christian Gluud, Margaret Cooney, Steffen Thirstrup, Wolfgang Kuchinke, Christine Kubiak, Sebastian Geismann, Christian Libersa
Publikováno v:
Trials
Trials, BioMed Central, 2012, 13 (1), pp.27. ⟨10.1186/1745-6215-13-27⟩
Trials, Vol 13, Iss 1, p 27 (2012)
Trials, BioMed Central, 2012, 13 (1), pp.27. ⟨10.1186/1745-6215-13-27⟩
Trials, Vol 13, Iss 1, p 27 (2012)
Background In order to facilitate multinational clinical research, regulatory requirements need to become international and harmonised. The EU introduced the Directive 2001/20/EC in 2004, regulating investigational medicinal products in Europe. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bfb9700d0dd53f6f85f645e37567f48
