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To Report or Not to Report: Exploring Healthy Volunteers’ Rationales for Disclosing Adverse Events in Phase I Drug Trials

BACKGROUND: Phase I trials test the safety and tolerability of investigational drugs and often use healthy volunteers as research participants. Adverse events (AEs) are collected in part through participants’ self-reports of any symptoms they experience during the trial. In some cases, experiencing...

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Detalhes bibliográficos
Publicado no:AJOB Empir Bioeth
Main Authors: McManus, Lisa, Fisher, Jill A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5976538/
https://ncbi.nlm.nih.gov/pubmed/29693508
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/23294515.2018.1469552
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