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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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| Main Authors: | , , , , , , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
BioMed Central
2014
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3996165/ https://ncbi.nlm.nih.gov/pubmed/24742228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-7-245 |
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