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___/___/___ Red Rocks Community College ___ Date Submitted Institutional Review Board File NumberContinuing Review QuestionnairePrincipal Investigator:Project Title:Federal Regulations mandate that
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How to fill out institutional review board

01
Familiarize yourself with the guidelines and requirements of the specific institutional review board (IRB) you will be submitting to.
02
Obtain the necessary application forms and templates from the IRB.
03
Clearly state the purpose of your research and the importance of conducting it ethically and responsibly.
04
Provide detailed information about the study design, including the methodology, sample size, recruitment plan, and data collection procedures.
05
Address potential risks and benefits associated with the research and explain how you will minimize any potential harm to participants.
06
Include informed consent forms that clearly outline the study objectives, procedures, potential risks, and voluntary participation.
07
Provide documentation of your qualifications and expertise in conducting the proposed research.
08
Create a data management plan that describes how you will handle, store, and protect the collected data.
09
Include any necessary supporting documents, such as questionnaires, surveys, or interview protocols.
10
Submit your completed application to the IRB and follow up with any requested revisions or additional information.

Who needs institutional review board?

01
Researchers who are conducting studies involving human participants.
02
Academic institutions, hospitals, and other organizations that oversee and regulate research involving human subjects.
03
Ethics committees and review boards responsible for ensuring the protection and welfare of research participants.
04
Studies funded by government agencies or private organizations that require ethical oversight.

What is Institutional Review Board - Frequently Asked Questions Form?

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An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects, ensuring that their rights and welfare are protected.
Researchers who plan to conduct studies involving human participants are required to submit their research proposals to an IRB for review.
To fill out an IRB application, researchers typically need to provide information about the study's purpose, methodology, participant recruitment, consent procedures, and potential risks involved.
The purpose of an IRB is to protect the rights, welfare, and well-being of research participants by ensuring that the study follows ethical guidelines.
Researchers must report details such as study design, participant demographics, informed consent processes, potential risks and benefits, and data confidentiality measures.
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