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The research summary is included as part of your IRB application. In addition to this summary you will need to complete a Request for IRB Review form. For more information about the IRB process, please
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How to fill out irb research summary exemplar

01
To fill out the IRB research summary exemplar, follow these steps:
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Start by providing the title of your research project.
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Next, provide a brief and concise summary of your research objectives.
04
Describe the methodology or approach you will use in your research.
05
Provide an overview of your research participants and how you plan to recruit them.
06
Explain any potential risks or benefits associated with your research.
07
Describe the data collection and analysis procedures you will employ.
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Discuss any anticipated outcomes or findings of your research.
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Include information about any external collaborations or funding sources.
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Finally, review your completed exemplar for accuracy and completeness before submitting it.

Who needs irb research summary exemplar?

01
The IRB research summary exemplar is typically required by researchers and institutions who conduct studies involving human participants and need to obtain approval from an Institutional Review Board (IRB). It helps to provide a comprehensive overview of the research project, ensuring ethical considerations and participant safety are taken into account.
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The IRB research summary exemplar is a brief overview of a research study that provides key information for review by the Institutional Review Board (IRB).
Researchers conducting studies involving human subjects are required to file an IRB research summary exemplar.
To fill out an IRB research summary exemplar, researchers need to provide information such as study objectives, methodology, risks and benefits, and informed consent procedures.
The purpose of an IRB research summary exemplar is to help the IRB assess the ethical and methodological aspects of a research study involving human subjects.
Key information that must be reported on an IRB research summary exemplar includes study objectives, methods, risks and benefits, and informed consent procedures.
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