“Ready-to-Recruit” or “Ready-to-Consent” Populations? Informed Consent and the Limits of Subject Autonomy

This article queries the pharmaceutical industry's concept of “ready-torecruit” populations by examining its recruitment strategies for clinical trials and the types of human subjects who participate in these drug studies. The argument is that the pharmaceutical industry has profited from a sys...

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Bibliographic Details
Published in:	Qualitative inquiry Vol. 13; no. 6; pp. 875 - 894
Main Author:	Fisher, Jill A.
Format:	Journal Article
Language:	English
Published:	Los Angeles, CA SAGE Publications 01.09.2007 SAGE PUBLICATIONS, INC
Subjects:	Alternative approaches Autonomy Clinical research Clinical trial Clinical trials Consensus Drug industry Drugs Ethical standards Ethics Human subjects Informed consent Meaning Medical ethics Medical Research Medicine Motivation Participants Participation Pharmaceutical industry Pharmaceuticals Pharmacy Population Populations Qualitative analysis Qualitative research Recruitment Regulation Research Ethics Research subjects Researcher Subject Relations U.S.A Vulnerability Vulnerable people pharmaceutical industry human subjects clinical trials informed consent recruitment
ISSN:	1077-8004, 1552-7565
Online Access:	Get full text
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