Assessing for quality informed consent with subjects enrolling in clinical research /

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

Main Author:	Holtz, Laura R. (Author)
Other Authors:	Byrdsong, Quincy (Editor)
Format:	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. Research Design Consentement éclairé (Droit médical) > Recherche. Médecine clinique > Recherche.
Online Access:	Connect to the full text of this electronic book