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IRB Process Classroom Projects Under Research Methodology Courses DOCUMENT CONTROL Prepared by: Karen BaroudyDepartment/Division: Department of Graduate Studies and Research, IRB Office Approved by: Pierre
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How to fill out irb process

01
Review the IRB application form and instructions to understand the information required.
02
Ensure that you have all the necessary supporting documents and materials.
03
Complete each section of the IRB application form accurately and thoroughly, providing all requested information.
04
Include any relevant supporting documentation such as informed consent forms, recruitment materials, and study protocols.
05
Provide detailed information regarding the study design, research objectives, and methods to be used.
06
Explain the potential risks and benefits of the research to participants.
07
Include information on how you plan to protect participant privacy and confidentiality.
08
Submit the completed IRB application form and supporting documents to the appropriate IRB office.
09
Respond promptly and accurately to any requests for additional information or clarifications from the IRB.
10
Await notification from the IRB regarding approval or any necessary revisions.
11
Make any required changes or modifications to the research protocol as directed by the IRB.
12
Once approved, ensure compliance with all IRB requirements throughout the duration of the study.

Who needs irb process?

01
Researchers who plan to conduct research involving human subjects.
02
Institutions and organizations that receive federal funding for research.
03
Students and faculty members who are involved in academic research projects.
04
Individuals and organizations seeking to ethically and responsibly conduct research involving human participants.
05
Researchers who want to ensure the protection of participant rights, safety, and well-being.
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The IRB process, or Institutional Review Board process, is a systematic method for reviewing and approving research projects involving human subjects.
Researchers conducting studies involving human subjects are required to file an IRB process.
Researchers must submit a detailed research protocol to the IRB for review and approval.
The purpose of the IRB process is to ensure the protection of human subjects involved in research studies.
The IRB process must include details on the research protocol, potential risks to participants, informed consent process, and plans for protecting participants.
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