Reducing Clinical Trial Monitoring Resources and Costs With Remote Monitoring: Retrospective Study Comparing On-Site Versus Hybrid Monitoring

BACKGROUND: Clinical research associates (CRAs) monitor the progress of a trial, verify the data collected, and ensure that the trial is carried out and reported in accordance with the trial protocol, standard operating procedures, and relevant laws and regulations. In response to monitoring challen...

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Detalles Bibliográficos
Autores principales: Fu, Zhiying, Liu, Xiaohong, Zhao, Shuhua, Yuan, Yannan, Jiang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2023
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337412/
https://www.ncbi.nlm.nih.gov/pubmed/37368468
http://dx.doi.org/10.2196/42175

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337412/
https://www.ncbi.nlm.nih.gov/pubmed/37368468
http://dx.doi.org/10.2196/42175

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