Enrollment in research under exception from informed consent: The Patients’ Experiences in Emergency Research (PEER) study

Author:

Dickert Neal W.,Mah Victoria A.,Baren Jill M.,Biros Michelle H.,Govindarajan Prasanthi,Pancioli Arthur,Silbergleit Robert,Wright David W.,Pentz Rebecca D.

Funder

National Institute of Neurological Disorders and Stroke

National Institutes of Health

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Emergency,Emergency Medicine

Reference22 articles.

1. U.S. Food and Drug Administration. Title 21 (Code of Federal Regulations), Part 50.24 Protection of Human Subjects 2004.

2. U.S. Department of Health and Human Services and Food and Drug Administration. Guidance for Institutional Review Boards, clinical investigators, and sponsors: exception from informed consent requirements for emergency research. 2011; http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM249673.pdf. Accessed January 24, 2013, 2012.

3. Is emergency research without initial consent justified? The consent substitute model;Largent;Arch Intern Med,2010

4. The research on community consultation: an annotated bibliography;Baren;Acad Emerg Med,2007

5. Research without consent: community perspectives from the Community VOICES Study;Richardson;Acad Emerg Med,2005

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