Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Margarete, Heiden"'
Publikováno v:
Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 58:1247-1253
In order to address the European Directive 2004/23 on human tissues and cells, the authorization obligation for tissue and blood stem cell preparations was introduced (§ 21a AMG) in the year 2007 in the German medicinal products act. Stem cell trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fd89316f7e46d4d14b74f6421598780
https://doi.org/10.1007/s00103-015-2241-3
https://doi.org/10.1007/s00103-015-2241-3
Publikováno v:
Transfusion Medicine and Hemotherapy. 37:29-47
The present report contains the data collected in 2007, pursuant to Section 21 German Transfusion Act, and an analysis of the supply situation over the past 8 years. As in previous years, all blood donation centres located in Germany transmitted data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5aec02f634aac9f61df09b7820d8147
https://doi.org/10.1159/000269555
https://doi.org/10.1159/000269555
Autor:
Ute, Vahlensieck, Susanne, Poley-Ochmann, Anneliese, Hilger, Margarete, Heiden, Rainer, Seitz
Publikováno v:
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz. 58(11-12)
In order to address the European Directive 2004/23 on human tissues and cells, the authorization obligation for tissue and blood stem cell preparations was introduced (§ 21a AMG) in the year 2007 in the German medicinal products act. Stem cell trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::14dd40878e4b0b9f7b4fb360125f081a
https://pubmed.ncbi.nlm.nih.gov/26459568
https://pubmed.ncbi.nlm.nih.gov/26459568
Autor:
Rainer Seitz, Margarete Heiden
Publikováno v:
Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 42:150-155
Im Gegensatz zu den Regelungen in anderen europaischen Landern werden in Deutschland Blutkomponenten zur Transfusion durch das Arzneimittelgesetz den Arzneimiteln zugeordnet; fur die ist eine Zulassung erforderlich. Da es sich bei Blutkomponenten um
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b8e9f4eabbf3f86d804b7979b4643a9
https://doi.org/10.1007/s001030050076
https://doi.org/10.1007/s001030050076
Autor:
Utta Schurig, Helga Huber, Margarete Heiden, Egbert Flory, Thomas Montag, Michael Schwanig, Ralf Sanzenbacher, Sven-Boris Nicol, Christian Schneider
Publikováno v:
Clinical Chemistry and Laboratory Medicine. 46
Today, sterility of established parenteral drugs including biologicals, such as plasma derived products, is practically guaranteed. Bacterially contaminated products are extremely rare exceptions owing to the efficiency of the manufacturing processes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81264862570442ac349bfaebe39bf5c5
https://doi.org/10.1515/cclm.2008.175
https://doi.org/10.1515/cclm.2008.175