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GCP inspections in Germany and Europe following the implementation of the Directive 2001/20/EC

Background: The implementation of the Clinical Trials Directive 2001/20/EC and the Good Clinical Practice Directive 2005/28/EC fundamentally restructured and harmonized the conduct of clinical trials in Europe. GCP inspections – which affect study sites, laboratories, sponsors and contract research...

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Dettagli Bibliografici
Autori principali: Göbel, Claus, Baier, Dieter, Ruhfus, Birgit, Hundt, Ferdinand
Natura: Artigo
Lingua:Inglês
Pubblicazione: German Medical Science GMS Publishing House 2009
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2716552/
https://ncbi.nlm.nih.gov/pubmed/19675741
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3205/000060
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