Legal and ethical policies regarding research involving critically ill children

Virtual Mentor

Volumn 14, Issue 10, 2012, Pages 797-800

  Koogler, Tracy ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CRITICAL ILLNESS; DECISION MAKING; EMERGENCY HEALTH SERVICE; ETHICS; HUMAN; HUMAN EXPERIMENT; INFORMED CONSENT; INTENSIVE CARE; LEGAL ASPECT; MEDICAL ETHICS; PARENTAL CONSENT; PATIENT SELECTION; RISK ASSESSMENT; TREATMENT OUTCOME; UNITED STATES;

CHILD; CRITICAL ILLNESS; DECISION MAKING; EMERGENCY MEDICAL SERVICES; ETHICS, MEDICAL; HUMAN EXPERIMENTATION; HUMANS; INFORMED CONSENT BY MINORS; INTENSIVE CARE; PARENTAL CONSENT; PATIENT SELECTION; RISK ASSESSMENT; TREATMENT OUTCOME; UNITED STATES;

EID: 84882696957     PISSN: 19377010     EISSN: None     Source Type: Journal    
DOI: 10.1001/virtualmentor.2012.14.10.pfor1-1210     Document Type: Review

References (4)

1. Department of Health and Human Services. Basic HHS Policy for Protection of Human Subjects (Common Rule), 45 CFR part 46 subpart D.
2. Food and Drug Administration Office of Good Clinical Practice. Guidance for institutional review boards, clinical investigators, and sponsors: exception from informed consent requirements for emergency research. http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM249673.pdf. Accessed September 10, 2012.
3. Nelson RM. Challenges in the conduct of emergency research in children: a workshop report. Am J Bioeth. 2006;6(6):W1-W9.
4. Ross LF. Children in Medical Research: Access versus Protection. New York: Oxford University Press: 2006.