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- W127383177 abstract "Good Clinical Practice (GCP) is an internationally adoptedstandard for clinical trials, and one important component ofthis document is the requirement that investigators informtrial sponsors of serious adverse events, defined as ‘‘anyuntoward medical occurrence that results in hospitalizationor prolongation of hospitalization, or is life-threatening, orresults in death or disability, including birth defects.’’" @default.
- W127383177 created "2016-06-24" @default.
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- W127383177 date "2012-08-31" @default.
- W127383177 modified "2023-10-09" @default.
- W127383177 title "Failure to report harms and adverse events in clinical trials: Why does the problem continue?" @default.
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- W127383177 doi "https://doi.org/10.1007/s12630-012-9777-6" @default.
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