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Use for continuing review OR as a final report to close a study. Is this a renewal or a closure? IRB project # and study titleInvestigator: Department:Physical address, phone #, and email address:
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How to fill out use for continuing review

01
Step 1: Gather all relevant information and documents related to the continuing review process.
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Step 2: Review the current use and any changes or updates that need to be made.
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Step 3: Fill out the necessary forms or templates provided by the organization or institution.
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Step 4: Provide detailed information about the study objectives, methods, risks, and benefits.
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Step 5: Explain any changes or amendments to the previous use for continuing review.
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Step 6: Include any necessary supporting documents or evidence to support the review process.
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Step 7: Submit the completed application for continuing review, either online or through the designated submission process.
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Step 8: Follow up and respond to any additional requests or clarifications from the reviewing committee or board.
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Step 9: Review and comply with any feedback or recommendations provided by the reviewing committee.
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Step 10: Maintain accurate records and documentation of the continuing review for future reference or auditing purposes.

Who needs use for continuing review?

01
Researchers who are conducting studies involving human subjects and are required to undergo continuing review by an institutional review board (IRB) or ethics committee.
02
Institutions or organizations that have policies or regulations in place requiring continuing review for research involving human subjects.

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Use for continuing review is a process conducted by research institutions to ensure that research involving human subjects continues to meet ethical and regulatory standards.
Principal Investigators and research teams conducting studies involving human subjects are required to file use for continuing review.
Use for continuing review forms can typically be filled out online or on paper, and require information about the study protocol, any changes made since initial approval, and documentation of ongoing consent procedures.
The purpose of use for continuing review is to ensure the ongoing safety and well-being of human subjects participating in research studies, as well as to maintain compliance with ethical and regulatory standards.
Information that must be reported on use for continuing review includes any changes to the study protocol, documentation of ongoing consent procedures, adverse events, and any new information that may affect the risks and benefits of the study.
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