Use of Human Subjects in Research  

Federalwide Assurance  
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In exercising their authority, IRBs may approve, disapprove, or table research protocols. However, IRBs are obligated not to approve any protocol that does not meet the criteria previously presented.



Most often, the IRB approves a research protocol with required changes. Research may not begin until the changes have been met in writing by the Protocol Director and approved by the IRB.



This completes the FWA module of this tutorial. The "Next" button below will advance you to the module on individual and organizational roles and responsibilities.

 

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