The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating for the subject's right ...
Potential research subjects must be accurately informed of what a project involves, and given the opportunity to decide of their own free will whether or not to participate. This process may be brief ...
Journal of Empirical Research on Human Research Ethics: An International Journal, Vol. 16, No. 1/2 (February-April 2021), pp. 78-88 (10 pages) HIV cure research carries serious risks and negligible ...
Canadian researchers have published new guidelines intended to make consent forms used in clinical research easier for patients to understand. The guidelines describe 75 core elements for consent ...
Researchers reported on patient acceptance of an e-consent tool for asynchronous delivery of study information and for receiving consent from patients.
The primary purpose of informed consent is to protect the prospective human subject. Informed consent provides the individual with the pertinent information regarding the research in which s/he is ...
Federal regulations require that researchers obtain legally effective, documented, voluntary informed consent from prospective subjects (or subjects' legally authorized representatives) before ...
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