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This document serves as an application packet for the Institutional Review Board (IRB) review of research projects involving human subjects, including the submission of necessary forms for approval
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How to fill out institutional review board application

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How to fill out INSTITUTIONAL REVIEW BOARD APPLICATION PACKET

01
Collect all necessary documents required for the application.
02
Complete the Application Form, providing detailed information about the study.
03
Outline the study's purpose and significance in the section provided.
04
Describe the methodology you will use in your research.
05
Include information on the study population, including how participants will be recruited.
06
Detail the potential risks and benefits to participants.
07
Include a data management and privacy plan.
08
Provide consent forms and describe the consent process.
09
Ensure that all team members sign the application where required.
10
Submit the completed application and wait for confirmation of receipt.

Who needs INSTITUTIONAL REVIEW BOARD APPLICATION PACKET?

01
Researchers conducting studies involving human subjects.
02
Graduate students working on thesis or dissertation research.
03
Faculty members engaging in scholarly research.
04
Organizations conducting clinical trials or social science research.
05
Any institution that receives funding or support for research activities.
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IRBs must have at least five members, including at least one scientist, one non-scientist, and one member who is not affiliated with the institution. The non-affiliated member should not be part of the immediate family of a person who is affiliated with the institution.
IRB Members Sr.NoPrimary MembersAlternate Members 1 Ashwini Chhatre (Chair, IRB) D V R Seshadri (Alternate Chair, IRB) 2 Raghuram Bommaraju Deepak Jena 3 Sanjay Kallapur Hemant Kakkar 4 Saumya Sindhwani Pallavi Basu2 more rows
The U.S. Federal policy requires that an IRB have at least 5 members of varying backgrounds including a chair person, a scientific member, a non‐scientific member, a representative of the community not affiliated with the institution, and a member of the institution.
21 CFR 56.107(c) requires at least one member of the IRB to have primary concerns in the scientific area and at least one to have primary concerns in the non-scientific area. Most IRBs include physicians and Ph. D. level physical or biological scientists.
Each IRB committee will include at least one member who represents the perspective of research participants. Each IRB committee will include at least one member whose primary concerns are in scientific areas and at least one member whose primary concerns are in non-scientific areas.
If your study is more than minimal risk, it will be harder for you to get IRB approval. You will need to justify why you are running the study. Less common types of risk for psychology studies are social, physical, and financial.
The quick list: Complete CITI training if you are not up to date. Prepare all your documents (consent, stimuli & materials, surveys, recruitment) beforehand. Go to your institution's IRB app site. Read carefully. Follow the instructions. Answer clearly. Don't be wordy. Whenever possible, give yourself wiggle room.
Checklists are used by the IRB staff and reviewers to document required IRB determinations. Investigators may consult the checklists to understand the regulatory requirements related to research, however, Investigators are not required to complete the checklists: HRP-410 - Waiver or Alteration of the Consent Process.

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The Institutional Review Board Application Packet is a collection of forms and documents that researchers must complete and submit to an Institutional Review Board (IRB) to seek approval for research involving human subjects.
Researchers, faculty members, or students conducting research involving human subjects in institutions that require IRB oversight are required to file the Institutional Review Board Application Packet.
To fill out the Institutional Review Board Application Packet, researchers should carefully read the instructions provided, complete each section accurately, provide detailed information about the study design and methodology, and submit any additional required documents.
The purpose of the Institutional Review Board Application Packet is to ensure that research involving human subjects is conducted ethically, safeguards the rights and welfare of participants, and complies with federal regulations.
The information that must be reported on the Institutional Review Board Application Packet includes study objectives, research methodology, participant recruitment strategies, informed consent processes, potential risks to participants, and data management plans.
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