Standard requirements for GCP-compliant data management in multinational clinical trials

BACKGROUND: A recent survey has shown that data management in clinical trials performed by academic trial units still faces many difficulties (e.g. heterogeneity of software products, deficits in quality management, limited human and financial resources and the complexity of running a local computer...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ohmann, Christian, Kuchinke, Wolfgang, Canham, Steve, Lauritsen, Jens, Salas, Nader, Schade-Brittinger, Carmen, Wittenberg, Michael, McPherson, Gladys, McCourt, John, Gueyffier, Francois, Lorimer, Andrea, Torres, Ferràn
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2011
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3074516/
https://ncbi.nlm.nih.gov/pubmed/21426576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1745-6215-12-85
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