Human health research ethics

Science

Volumn 305, Issue 5686, 2004, Pages 949-

  Silbergeld, E ^a   Lerman, S ^b   Hushka, L ^b  

^a JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^b EXXONMOBIL UPSTREAM RESEARCH COMPANY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEDICINE;

DECISION MAKING; MEDICAL ETHICS; MEDICAL RESEARCH; POLICY; PRIORITY JOURNAL; RESEARCH SUBJECT; SHORT SURVEY; STANDARD; ADVISORY COMMITTEE; ARTICLE; BIOETHICS; BIOMEDICAL AND BEHAVIORAL RESEARCH; CLINICAL TRIAL; ETHICS; FEDERAL POLICY (COMMON RULE) FOR THE PROTECTION OF HUMAN SUBJECTS 1991; GOVERNMENT; GOVERNMENT REGULATION; HUMAN; HUMAN EXPERIMENT; LEGAL APPROACH; ORGANIZATION; PROFESSIONAL STANDARD; RESEARCH ETHICS; TOXICITY TESTING; UNITED STATES;

BIOMEDICAL AND BEHAVIORAL RESEARCH; FEDERAL POLICY (COMMON RULE) FOR THE PROTECTION OF HUMAN SUBJECTS 1991; LEGAL APPROACH;

ADVISORY COMMITTEES; BIOETHICAL ISSUES; CLINICAL TRIALS; ETHICS COMMITTEES, RESEARCH; ETHICS, RESEARCH; GOVERNMENT REGULATION; HUMAN EXPERIMENTATION; HUMANS; NATIONAL ACADEMY OF SCIENCES (U.S.); PUBLIC POLICY; RESEARCH SUBJECTS; TOXICITY TESTS; UNITED STATES; UNITED STATES ENVIRONMENTAL PROTECTION AGENCY;

EID: 4243137328     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1096862     Document Type: Short Survey

References (9)

1. Science Advisory Board and the FIFRA Scientific Advisory Panel, EPA, "Comments on the use of data from the testing of human subjects" (EPA-SAB-EC-00-017, EPA, Washington, DC, 2000).
2. EPA, Agency requests National Academy of Sciences input on consideration of certain human toxicity studies; announces interim policy (press release, 14 December 2001).
3. National Research Council (NRC). Use of Third-Party Toxicity Research with Human Research Participants (National Academies Press, Washington, DC, 2002).
4. EPA, Human testing; Advance notice of proposed rule-making, Docket no. OPP-2003-0132, Fed. Regist. 68, 24410 (2003).
5. DHHS, Protection of human subjects, Code of Federal Regulations (CFR) 40, part 26 (2001).
6. World Medical Association, "Declaration of Helsinki: Ethical principles for medical research involving human subjects" (World Medical Association, Edinburgh, 2000).
7. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH Topic E6: Guideline for Good Clinical Practice, Geneva, 1996).
8. NRC, Intentional Human Dosing Studies for EPA Regulatory Purposes: Scientific and Ethical Issues (National Academies Press, Washington, DC, 2004).
9. The Council for international Organizations of Medical Sciences (CIOMS), International Ethical Guidelines for Biomedical Research Involving Human Subjects (National Academies Press, Washington, DC, 2002).