Determination of required content of the informed consent process for human participants in biomedical research conducted in the U.S.: A practical tool to assist clinical investigators

Contemporary Clinical Trials

Volumn 29, Issue 4, 2008, Pages 501-506

  Chanaud, Cheryl M ^a  

^a MEMORIAL HERMANN HOSPITAL   (United States)

Author keywords

Federal law; Informed consent; International guidelines

Indexed keywords

ARTICLE; DOCUMENT EXAMINATION; INFORMED CONSENT; LAW; MEDICAL ETHICS; MEDICAL RESEARCH; PRACTICE GUIDELINE; UNITED STATES;

BIOMEDICAL RESEARCH; ETHICS, RESEARCH; GOVERNMENT REGULATION; GUIDELINES AS TOPIC; HUMANS; INFORMED CONSENT; PATIENT SELECTION; RESEARCH PERSONNEL; UNITED STATES;

EID: 44049091313     PISSN: 15517144     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cct.2007.11.006     Document Type: Article

References (13)

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12. www.ich.org/cache/compo/276-254-1.html. September 2002.
13. International guidelines for Biomedical Research involving human subjects. CIOMS (2002). www.cioms.ch/frame_guidelines_nov_2002.htm