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Informed consent: Are we doing enough?

The process of informed consent is an ethical mandate for all clinical trials. The principles of ethics in research involving human beings decrees the conduct of a process where the prospective research subjects should be informed of all aspects of the research study and after complete comprehension...

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Detalhes bibliográficos
Autor principal: Pranati
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3043361/
https://ncbi.nlm.nih.gov/pubmed/21350726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-3485.71769
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