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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Clin Trials
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2015
Gaiak:
Article
Sarrera elektronikoa: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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