E-book
Tri-council policy statement ethical conduct for research involving humans
Record details
- ISBN: 9780662402367 (electronic bk.)
- ISBN: 0662402367 (electronic bk.)
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Physical Description:
electronic resource
remote
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1 electronic text (1 v. (various pagings)) : digital file. - Edition: Aug. 1998, with 2000, 2002, 2005 amendments.
- Publisher: Ottawa, Ont. : Interagency Secretariat on Research Ethics, c2005
Content descriptions
| General Note: | Issued as part of the desLibris documents collection. |
| Bibliography, etc. Note: | Includes bibliographical references. |
| Formatted Contents Note: | Introduction -- Goals of the policy -- A. Mandate of the agencies -- B. Goals and rationale of the policy -- Context of an ethics framework -- A. The need for research -- B. A moral imperative : respect for human dignity -- C. Guiding ethical principles -- D. A subject-centred perspective -- E. Academic freedoms and responsibilities -- F. Ethics and law -- G. Putting principles into practice -- section 1. Ethics review -- A. Research requiring ethics review -- B. Research ethics boards (REBs) -- C. Analysis, balance and distribution of harms and benefits -- D. Review procedures -- E. Conflicts of interest -- F. Review procedures for ongoing research -- G. Review of multicentred research -- H. Review of research in other jurisdictions or countries -- section 2. Free and informed consent -- A. Requirement for free and informed consent -- B. Voluntariness -- C. Naturalistic observation -- D. Informing potential subjects -- E. Competence -- F. Research in emergency health situations -- section 3. Privacy and confidentiality -- A. Accessing private information : personal Interviews -- B. Accessing private information : surveys, questionnaires and the collection of data -- C. Secondary use of data -- D. Data linkage -- section 4. Conflict of interest -- A. Conflicts of interest involving researchers -- B. Conflicts of interest by REB members -- C. Institutional conflicts of interest -- section 5. Inclusion in research -- A. Introduction -- B. Research involving women -- C. Research involving those who are incompetent to consent for themselves -- section 6. Research involving Aboriginal peoples -- A. Introduction -- B. Good practices -- section 7. Clinical trials -- A. Clinical equipoise -- B. Phases of pharmaceutical research -- C. Multicentre clinical trials -- D. Placebo-controlled studies -- E. Analysis and dissemination of the results of clinical trials -- section 8. Human genetic research -- A. The individual, families and biological relatives -- B. Privacy, confidentiality, loss of benefits and other harms -- C. |
| System Details Note: | Mode of access: World Wide Web. |
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