Difference between revisions of "Human Subjects Approval"
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All impact evaluations must be fully compliant with both local and international Institutional Review Boards (IRB). | |||
All members of the research team who will manage surveys and work with personally identified data must complete training on conducting research with human subjects | Local IRB approvals vary by country; research local regulations when the impact evaluation is designed. | ||
International IRB approvals: The World Bank does not have an IRB. Typically, IRB approval is sought from partner academic / research organizations (e.g. universities, Innovation for Poverty Action). | |||
All members of the research team who will manage surveys and work with personally identified data must complete training on conducting research with human subjects. The National Institute for Health (NIH) offers a free course on "Protecting Human Research Participants". [https://phrp.nihtraining.com/users/login.php] | |||
All surveys require informed consent from every respondent. See an example Informed Consent module [here]. | |||
Revision as of 17:17, 13 January 2017
All impact evaluations must be fully compliant with both local and international Institutional Review Boards (IRB).
Local IRB approvals vary by country; research local regulations when the impact evaluation is designed.
International IRB approvals: The World Bank does not have an IRB. Typically, IRB approval is sought from partner academic / research organizations (e.g. universities, Innovation for Poverty Action).
All members of the research team who will manage surveys and work with personally identified data must complete training on conducting research with human subjects. The National Institute for Health (NIH) offers a free course on "Protecting Human Research Participants". [1]
All surveys require informed consent from every respondent. See an example Informed Consent module [here].