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Comprehensive Format of Informed Consent in Research and Practice: A Tool to uphold the Ethical and Moral Standards
Informed consent in research, clinical trial, and practice is a process in which a patient/participant consents to participate or undergo the proposed procedures after being informed of its procedures, risks, and benefits. Ideally, the patient/participant is expected to give his consent only after f...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Jaypee Brothers Medical Publishers
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360808/ https://www.ncbi.nlm.nih.gov/pubmed/28377660 http://dx.doi.org/10.5005/jp-journals-10005-1411 |