Serious adverse events and compensation in registration trials: a review of data from a Japanese university hospital

BACKGROUND: Clinical trials leading to regulatory approval, or registration trials, play a central role in the development of drugs and medical devices. The contribution of support staff, such as the clinical research coordinator (CRC) and administrative officers, in registration trials is now widel...

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Detalles Bibliográficos
Autores principales: Watanabe, Miho, Tajima, Soichiro, Katashima, Rumi, Miyamoto, Toshiko, Yamagami, Makiko, Minakuchi, Kazuo, Yanagawa, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996165/
https://www.ncbi.nlm.nih.gov/pubmed/24742228
http://dx.doi.org/10.1186/1756-0500-7-245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996165/
https://www.ncbi.nlm.nih.gov/pubmed/24742228
http://dx.doi.org/10.1186/1756-0500-7-245

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