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What if I am enrolling NIH subjects who will never be physically seen at an NIH site?
Use the template below if you are enrolling NIH subjects off-site; meaning these people will never come to an NIH site to be seen as a participant. For example, a field cohort or participants who are entirely remote where there is no physical contact with that person, or participants that are seen at non-traditional locations such as a church or community hall. If you are using Clinical Center resources in any way for the protocol (this includes using iMed for consent or sending in samples to an NIH CC lab for analysis) then you cannot use this template and you would need to use the Clinical Center consent template instead for your protocol. It should be used in cases where the NIH Institutional Review Board (IRB) is the Reviewing IRB for this protocol.
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If you need a 508 compliant version of a template that can be read by a screen reader, please contact the IRB Office by email at IRB@od.nih.gov. |
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