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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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Detalhes bibliográficos
Publicado no:Clin Trials
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha: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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