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International ethical guidelines for biomedical research involving human subjects
2002, CIOMS, World Health Organization
in English
9290360755 9789290360759
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Book Details
Table of Contents
1. Ethical justification and scientific validity of biomedical research involving human subjects
2. Ethical review committees
3. Ethical review of externally sponsored research
4. Individual informed consent
5. Obtaining informed consent: Essential information for prospective research subjects
6. Obtaining informed consent: Obligations of sponsors and investigators
7. Inducement to participate in research
8. Benefits and risks of study participation
9. Special limitations on risk when research involves individuals who are not capable of giving informed consent
10. Research in populations and communities with limited resources
11. Choice of control in clinical trials
12. Equitable distribution of burdens and benefits in the selection of groups of subjects in research
13. Research involving vulnerable persons
14. Research involving children
15. Research involving individuals who by reason of mental or behavioural disorders are not capable of giving adequately informed consent
16. Women as research subjects
17. Pregnant women as research subjects
18. Safeguarding confidentiality
19. Right of injured subjects to treatment and compensation
20. Strengthening capacity for ethical and scientific review of biomedical research
21. Ethical obligation of external sponsors to provide health-care services.
Edition Notes
"This is the third in the series of international ethical guidelines for biomedical research involving human subjects issued by the Council for International Organizations of Medical Sciences (CIOMS) since 1982.-- Introd.
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