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Institutional Review Board Standard Operating Procedure Document Code: IRBSOP1120IPR00206 Chapter II : Initial Protocol Review and Approval Effective Date: Page: November 23, 2020 Page 1 of 75 Issued

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How to fill out institutional review board

01

Submit application: Fill out the required institutional review board application forms

02

Provide necessary documents: Include protocol, consent forms, research instruments, and any other relevant materials

03

Ensure ethical standards: Clearly outline the ethical considerations of the research study

04

Submit for review: Submit the completed application and documents to the institutional review board for evaluation

05

Follow up: Address any feedback or clarifications requested by the board before proceeding with the research

Who needs institutional review board?

01

Researchers conducting studies involving human subjects

02

Institutions or organizations carrying out research projects that involve human participants

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What is institutional review board?

An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects, ensuring that the study complies with ethical standards and federal regulations.

Who is required to file institutional review board?

Researchers conducting studies involving human subjects, including faculty, staff, and students associated with an institution, are required to file for IRB approval.

How to fill out institutional review board?

To fill out an IRB application, researchers typically need to complete a form that includes details about the study's purpose, methodology, participant recruitment, informed consent process, and measures to protect participant confidentiality.

What is the purpose of institutional review board?

The purpose of an Institutional Review Board is to protect the rights and welfare of human subjects involved in research by ensuring that appropriate ethical standards are upheld.

What information must be reported on institutional review board?

Researchers must report information such as research objectives, participant demographics, methods of data collection, risks to participants, and how informed consent will be obtained.

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