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CHECKLIST: Non-Significant Risk Device NUMBER DATE PAGE HRP-418 3/25/2014 1 of 1 The purpose of this checklist is to provide support for IRB members or the Designated ...
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Who needs checklist - non-significant risk:
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Researchers conducting non-significant risk studies. This checklist is typically required for those conducting research studies that pose minimal risks to participants.
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Institutional Review Boards (IRBs) or Ethics Committees. These committees review and approve research projects to ensure participant safety. They may require researchers to complete a checklist to assess if the proposed study falls under the non-significant risk category.
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What is checklist - non-significant risk?
Checklist - non-significant risk is a document used to assess if a research study qualifies for exemption from certain regulatory requirements due to the minimal risk involved.
Who is required to file checklist - non-significant risk?
Researchers conducting studies with minimal risk are required to file the checklist - non-significant risk.
How to fill out checklist - non-significant risk?
The checklist - non-significant risk should be completed by providing accurate information about the study design, participants, procedures, and risk level.
What is the purpose of checklist - non-significant risk?
The purpose of the checklist - non-significant risk is to determine if a research study meets the criteria for exemption from certain regulatory requirements based on minimal risk.
What information must be reported on checklist - non-significant risk?
The checklist - non-significant risk must include details about the study design, participant characteristics, data collection methods, and risk assessment.
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