The research subject advocate at minority clinical research centers: An added resource for protection of human subjects

Ethnicity and Disease

Volumn 15, Issue 4 SUPPL. 5, 2005, Pages

  Easa, David ^a   Norris, Keith ^b   Hammatt, Zoë ^a   Kim, Kari ^a   Hernandez, Esther ^b   Kato, Kambrie ^a   Balaraman, Venkataraman ^a   Ho, Tammy ^a   Shomaker, Samuel ^a  

^a UNIVERSITY OF HAWAII   (United States)

^b CHARLES R DREW UNIVERSITY OF MEDICINE AND SCIENCE   (United States)

Author keywords

Clinical research; Health disparities research; Human subjects; Minority populations; Research participant safety; Research subject advocate

Indexed keywords

ARTICLE; CLINICAL PROTOCOL; CLINICAL RESEARCH; HEALTH CARE ORGANIZATION; HUMAN RELATION; HUMAN RIGHTS; INFORMED CONSENT; MINORITY GROUP; PROFESSIONAL STANDARD; RESEARCH ETHICS; RESEARCH SUBJECT;

BIOMEDICAL RESEARCH; HUMAN EXPERIMENTATION; HUMANS; MINORITY GROUPS; NATIONAL INSTITUTES OF HEALTH (U.S.); PATIENT ADVOCACY; UNITED STATES;

EID: 29244470799     PISSN: 1049510X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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