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Page 1 of 2 IRB Supplemental Form I Multiply Adverse Events Reporting Form Principal Investigator: Study Number: Study Title: Date Submitted: a) Briefly describe the circumstances of this event: b)
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What is irb supplemental form i?
IRB supplemental form i is a form used to provide additional information or clarifications to an Institutional Review Board (IRB) regarding a research study.
Who is required to file irb supplemental form i?
Researchers conducting studies that involve human subjects are required to file IRB supplemental form i.
How to fill out irb supplemental form i?
IRB supplemental form i can be filled out by providing detailed information about the study, addressing any concerns raised by the IRB, and submitting any additional documents requested.
What is the purpose of irb supplemental form i?
The purpose of IRB supplemental form i is to ensure that the IRB has all the necessary information to properly review and approve a research study involving human subjects.
What information must be reported on irb supplemental form i?
Information such as study protocols, participant recruitment methods, data collection procedures, informed consent documents, and any changes made to the original study protocol must be reported on IRB supplemental form i.
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