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September 25, 2024In This Issue NEW: OIA October Office Hours NEW: Kuali IRB Notification Updates NEW: Identifiability of Data NEW: IRB Expectations on Justice, Equity, Diversity, and Inclusion Reminder:
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How to fill out preparing updates to irb

01
Gather all relevant data and documentation related to the research project.
02
Review the previous IRB submission and identify any changes or updates needed.
03
Fill out the necessary IRB forms, including any specific sections regarding changes.
04
Clearly describe the changes to the study in a concise manner.
05
Provide justifications for all updates and how they impact the study.
06
Ensure all signatures and approvals are obtained before submission.
07
Submit the updated IRB application by following the institution's submission procedures.

Who needs preparing updates to irb?

01
Researchers conducting studies involving human subjects.
02
Institutional Review Board members who review research proposals.
03
Research assistants and coordinators involved in managing studies.
04
Regulatory compliance officers within research institutions.
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Preparing updates to the Institutional Review Board (IRB) involves compiling and submitting necessary modifications or new information related to research protocols that have been previously approved by the IRB.
Researchers and investigators involved in studies that have been approved by the IRB are required to file updates whenever there are changes to the research protocol, study personnel, or any other significant aspects of the study.
To fill out preparing updates to the IRB, researchers should complete the designated forms provided by the IRB, ensuring all required fields are filled in accurately and all changes or new details are clearly outlined and justified.
The purpose of preparing updates to the IRB is to ensure that the board is kept informed about any changes that may affect the ethical considerations, risks, and benefits of the research, thereby safeguarding the welfare of human subjects.
Information that must be reported includes any changes to the research design, methodology, participant recruitment, informed consent process, study staff, risks to participants, and data analysis plans.
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