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Continuing×Review×Form1. To×renew×the×study: Complete×and×send×this×report×at least×30 days×prior×to the×approval×expiration×date The×PI or×Designee×must×complete×and×sign×this×report
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Provide all relevant information requested, such as study details, protocol changes, and any adverse events.
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Who needs continuing review formdocx?

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Any individual or organization involved in an ongoing research study that requires periodic review and approval would need to fill out the continuing review formdocx. This may include researchers, students, institutions, or companies conducting clinical trials, surveys, or any other form of research with human subjects.
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Continuing review formdocx is a document that must be submitted to the Institutional Review Board (IRB) for approval to continue a research project involving human subjects.
Researchers or study teams conducting research projects involving human subjects are required to file continuing review formdocx.
Continuing review formdocx should be filled out by providing updated information about the research project, any changes in procedures, and the status of informed consent from participants.
The purpose of continuing review formdocx is to ensure that research projects involving human subjects are being conducted ethically and in accordance with regulations and guidelines.
Information such as any adverse events, participant recruitment status, changes in study procedures, and updates on informed consent must be reported on the continuing review formdocx.
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