Patients prefer easy adverse event reporting: Observational study within clinical trial
Background Digital intervention safety is crucial for regulatory approval and clinical adoption. However, the evaluation and reporting of adverse events (AEs) in clinical trials are often insufficient. Digital qualitative self-reporting could enhance the detection of AEs, but patient preferences for...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publishing
2025-05-01
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| coleção: | Digital Health |
| Acesso em linha: | https://doi.org/10.1177/20552076251345894 |
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