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| | #REDIRECT [[Protecting Human Research Subjects]] |
| <span style="color:#ff0000"> '''NOTE: this article is only a template. Please add content!''' </span>
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| </span>
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| add introductory 1-2 sentences here
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| = Read First =
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| * include here key points you want to make sure all readers understand
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| = Guidelines =
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| * organize information on the topic into subsections. for each subsection, include a brief description / overview, with links to articles that provide details
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| = Back to Parent =
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| This article is part of the topic [[*topic name, as listed on main page*]]
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| = Additional Resources =
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| * list here other articles related to this topic, with a brief description and link
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| [[Category: *category name* ]]
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| All impact evaluations must be fully compliant with both local and international Institutional Review Boards (IRB).
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| Local IRB approvals vary by country; research local regulations when the impact evaluation is designed.
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| 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 [http://www.poverty-action.org/researchers/working-with-ipa/irb]).
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| 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]
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| All surveys require informed consent from every respondent. See an example Informed Consent module [here].
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