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Bayesian Modeling for the Detection of Adverse Events Underreporting in Clinical Trials
INTRODUCTION: Safety underreporting is a recurrent issue in clinical trials that can impact patient safety and data integrity. Clinical quality assurance (QA) practices used to detect underreporting rely on on-site audits; however, adverse events (AEs) underreporting remains a recurrent issue. In a...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer International Publishing
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278191/ https://www.ncbi.nlm.nih.gov/pubmed/34260043 http://dx.doi.org/10.1007/s40264-021-01094-8 |