Clinical Trials: Minimising source data queries to streamline endpoint adjudication in a large multi-national trial

BACKGROUND: The UK Clinical Trial Regulations and Good Clinical Practice guidelines specify that the study sponsor must ensure clinical trial data are accurately reported, recorded and verified to ensure patient safety and scientific integrity. The methods that are utilised to assess data quality an...

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Detalles Bibliográficos
Autores principales: Tolmie, Elizabeth P, Dinnett, Eleanor M, Ronald, Elizabeth S, Gaw, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115878/
https://www.ncbi.nlm.nih.gov/pubmed/21548932
http://dx.doi.org/10.1186/1745-6215-12-112

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115878/
https://www.ncbi.nlm.nih.gov/pubmed/21548932
http://dx.doi.org/10.1186/1745-6215-12-112

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