Assessing for quality informed consent with subjects enrolling in clinical research / Laura R. Holtz, Quincy Byrdsong.

Research subjects are asked to participate in the informed consent process before participating in research. The elements and regulatory requirements of informed consent are well documented. However, there is less known about the quality of informed consent discussions that are occurring with potent...

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Bibliographic Details

Online Access:	Full Text (via SAGE)
Main Author:	Holtz, Laura R. (Author)
Other Authors:	Byrdsong, Quincy (Editor)
Format:	Electronic eBook
Language:	English
Published:	London : SAGE Publications Ltd, 2020.
Series:	SAGE Research Methods Cases: Medicine and Health.
Subjects:	Informed consent (Medical law) > Research. Clinical medicine > Research.