The role of community consultation in the ethical conduct of research without consent

American Journal of Bioethics

Volumn 6, Issue 3, 2006, Pages 33-35

  Richardson, Lynne D ^a   Rhodes, Rosamond ^a   Ragin, Deborah ^b   Wilets, Ilene ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b MONTCLAIR STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD SUBSTITUTE; HEMOGLOBIN; POLYMERIZED HEMOGLOBIN;

CLINICAL TRIAL; EMERGENCY HEALTH SERVICE; EMERGENCY TREATMENT; ETHICS; HUMAN; INFORMED CONSENT; INTERPERSONAL COMMUNICATION; PROFESSIONAL STANDARD; PUBLIC RELATIONS; RESEARCH ETHICS; SHORT SURVEY; UNITED STATES;

BLOOD SUBSTITUTES; CLINICAL TRIALS; COMMUNITY-INSTITUTIONAL RELATIONS; DISCLOSURE; EMERGENCY SERVICE, HOSPITAL; EMERGENCY TREATMENT; ETHICS COMMITTEES, RESEARCH; ETHICS, RESEARCH; HEMOGLOBINS; HUMANS; INFORMED CONSENT; UNITED STATES;

EID: 33745084199     PISSN: 15265161     EISSN: 15360075     Source Type: Journal    
DOI: 10.1080/15265160600685853     Document Type: Short Survey

References (10)

1. Dickert, N., and J. Sugarman. 2005. Ethical goals of community consultation in research. American Journal of Public Health. 95(7): 1123-1127.
2. Holloway, K. F. C. 2006. Accidental communities: Race, emergency medicine and the problem of PolyHeme®. American Journal of Bioethics 6(3): 7-17.
3. Kipnis, K., N. M. P. King, and R. M. Nelson. 2006. An open letter to IRBs considering Northfield Laboratories' PolyHeme® trial. American Journal of Bioethics 6(3): 18-21.
4. Lillie-Blanton, M., R. M. Martinez, and A. Salganicoff. 2001. Site of medical care: Do racial and ethnic differences persist? Yale Journal of Health Policy, Law and Ethics 1: 15-32.
5. Richardson, L. D. 2005. The ethics of research without consent. Mount Sinai Journal of Medicine 72(4): 242-249.
6. Richardson, L. D., T. E. Quest, and S. Birnbaum. 2005. Communicating with communities about emergency research. Academic Emergency Medicine 12(11): 1064-1070.
7. Richardson, L. D., I. Wilets, D. F. Ragin, J. Holohan, M. Smirnoff, R. Rhodes, G. Winkel, M. Rodriguez, and E. Ricci. 2005. Research without consent: Community perspectives from the Community VOICES Study. Academic Emergency Medicine 12(11): 1082-1090.
8. Satcher, D. 2001. Commentary: Our commitment to eliminate racial and ethnic health disparities. Yale Journal of Health Policy, Law and Ethics 1: 1-14.
9. Schmidt, T. A., N. M. Delorio, and K. B. McClure. 2006. The meaning of community consultation. American Journal of Bioethics 6(3): 30-32.
10. U.S. Food and Drug Administration. 1996. Code of Federal Regulations, Title 21, Part 50.24 (a) (7).