The ethics and regulatory landscape of including vulnerable populations in pragmatic clinical trials

Policies have been developed to protect vulnerable populations in clinical research, particularly the US federal research regulations (45 CFR 46 subparts B, C, and D). These policies generally recognize vulnerable populations to include pregnant women, fetuses, neonates, children, prisoners, persons...

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Опубликовано в: :Clin Trials
Главные авторы: Welch, Mary Jane, Lally, Rachel, Miller, Jennifer E, Pittman, Stephanie, Brodsky, Lynda, Caplan, Arthur L, Uhlenbrauck, Gina, Louzao, Darcy M, Fischer, James H, Wilfond, Benjamin
Формат: Artigo
Язык:Inglês
Опубликовано: 2015
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4662375/
https://ncbi.nlm.nih.gov/pubmed/26374681
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774515597701
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