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IORG0000247
BORG #:
Institution: Northwestern University
Expires:OMB No. 09900279
Approved for use through February 28, 202212/16/2022U. S. Department of Health and Human Services (HHS)
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This form ensures that participants understand the purpose, risks, and benefits of the study, and provides legal documentation of their informed consent.
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What is state of form irb?
The state of form IRB is a regulatory document that organizations submit to provide information regarding their research involving human subjects to ensure ethical standards and compliance with regulations.
Who is required to file state of form irb?
Research institutions, universities, and any entity conducting studies involving human subjects are required to file the state of form IRB.
How to fill out state of form irb?
To fill out the state of form IRB, one should gather all necessary information about the study, including the research plan, participant details, informed consent processes, and submit the document to the Institutional Review Board for review.
What is the purpose of state of form irb?
The purpose of state of form IRB is to protect the rights and welfare of human participants in research, ensuring that ethical standards are upheld and that risks are minimized.
What information must be reported on state of form irb?
The information that must be reported includes the study's title, purpose, methodology, participant recruitment strategies, risks and benefits, consent procedures, and data management plans.
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