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Central data monitoring in the multicentre randomised SafeBoosC-III trial – a pragmatic approach
BACKGROUND: Data monitoring of clinical trials is a tool aimed at reducing the risks of random errors (e.g. clerical errors) and systematic errors, which include misinterpretation, misunderstandings, and fabrication. Traditional ‘good clinical practice data monitoring’ with on-site monitors increase...
Autores principales: | Olsen, Markus Harboe, Hansen, Mathias Lühr, Safi, Sanam, Jakobsen, Janus Christian, Greisen, Gorm, Gluud, Christian |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325420/ https://www.ncbi.nlm.nih.gov/pubmed/34332547 http://dx.doi.org/10.1186/s12874-021-01344-4 |
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