Zobrazeno 1 - 3
of 3
pro vyhledávání: '"L. Sobaga"'
Autor:
H. M. Huber, B. Hinloopen, L. Sobaga, T. Müller-Kuller, A. Aquilina, F. Delaney, M. Nightingale, K. Barotine-Toth, J. deWit, J. Ceulemans, Erhard Seifried, Giuliano Grazzini, Walid Sireis, J. M. Cardenas, Margarethe Heiden, J. P. Jansen van Galen, Christian Seidl, Zuzana Cermakova, S. Pupella, F. Teskrat
Publikováno v:
ISBT Science Series. 7:16-23
EuBIS, the European blood inspection system, is a collaborative effort of 27 representatives from 19 Member States (MS), including governmental institutions, blood establishments and competent authorities. EuBIS has been initiated by co-funding throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20d8456a47b7a355d3887f6b80cbd565
https://doi.org/10.1111/j.1751-2824.2012.01612.x
https://doi.org/10.1111/j.1751-2824.2012.01612.x
Autor:
M. Nightingale, W. Siegel, J. P. Jansen van Galen, P. S. Skrablin, J. Ceulemans, A. McMillan Douglas, B. Kaltenbrunner-Bernitz, B. Hinloopen, A. Aquilina, F. Teskrat, J. de Wit, Zuzana Cermakova, Christian Seidl, K. Barotine-Toth, F. Delaney, Margarethe Heiden, G. Grazzini, H. M. Huber, L. Sobaga, Erhard Seifried
Publikováno v:
ISBT Science Series. 6:46-51
Background and Objectives The Public Health Programme (Directorate General Sanco) gave impetus to the need for equivalent recognition of inspections of blood establishments among European Member States (MS) through the development and implementation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ec1e1d73084914f86b1499f54f77877
https://doi.org/10.1111/j.1751-2824.2011.01434.x
https://doi.org/10.1111/j.1751-2824.2011.01434.x
Autor:
T. Müller-Kuller, A. M. Douglas, J. de Wit, P. Costello, Christian Seidl, J. P. Van Galen, V. Brixner, W. Siegel, F. Delaney, M. Nightingale, Zuzana Cermakova, W. Sireis, L. Sobaga, M. O’Connell, Erhard Seifried
Publikováno v:
ISBT Science Series. 3:54-62
The European blood legislation has defined several key quality elements to achieve Good Manufacturing Practice (GMP) in the field of blood transfusion. During the recent years, the blood legislation is in the process of implementation throughout its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b15d7fddadcf8d3f6cc11dd60695480d
https://doi.org/10.1111/j.1751-2824.2008.00182.x
https://doi.org/10.1111/j.1751-2824.2008.00182.x