Institutional review board practices regarding assent in pediatric research

Pediatrics

Volumn 113, Issue 6 I, 2004, Pages 1747-1752

  Whittle, Amy ^a   Shah, Seema ^a   Wilfond, Benjamin ^a,b   Gensler, Gary ^c   Wendler, David ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c EMMES CORPORATION   (United States)

Author keywords

Child; IRB

Indexed keywords

ADULT; AGE DISTRIBUTION; FEMALE; FUNCTIONAL ASSESSMENT; HUMAN; INFORMED CONSENT; INTERVIEW; MAJOR CLINICAL STUDY; MALE; MEDICAL INFORMATION; MEDICAL PRACTICE; MEDICAL SOCIETY; PATIENT SELECTION; PEDIATRICS; PRIORITY JOURNAL; REVIEW; TELEPHONE;

BIOMEDICAL AND BEHAVIORAL RESEARCH; EMPIRICAL APPROACH;

BIOMEDICAL RESEARCH; CHILD; DATA COLLECTION; ETHICS COMMITTEES, RESEARCH; GOVERNMENT REGULATION; HUMANS; INFORMED CONSENT; MENTAL COMPETENCY; REWARD; UNITED STATES;

EID: 2542643189     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.113.6.1747     Document Type: Review

References (11)

1. Department of Health and Human Services. United States Federal Regulations, 45 CFR 46, Subpart D (1991)
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