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INSTITUTIONAL REVIEW BOARD (IRB) CONTINUING REVIEW FORM FOR NONEXEMPT Studies continuing review is required for your study, please complete this form and submit it with current protocol materials
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How to fill out continuing review form for

01
Gather all necessary information such as protocol number, study title, principal investigator, and expiration date.
02
Review the current protocol and study procedures to ensure accuracy.
03
Complete any required sections on the continuing review form, including any updates or changes to the study.
04
Obtain necessary signatures from the principal investigator and other relevant parties.
05
Submit the completed continuing review form to the appropriate regulatory body by the deadline.

Who needs continuing review form for?

01
Researchers conducting clinical trials or studies that require ongoing review of protocols and procedures.
02
Institutions and regulatory bodies overseeing research activities.

What is CONTINUING REVIEW FOR NONEXEMPT STUDIES INVOLVING HUMAN Form?

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The continuing review form is used to assess ongoing research studies to ensure they continue to meet ethical standards and regulatory requirements throughout the study period.
Researchers or principal investigators conducting ongoing studies involving human subjects are typically required to file a continuing review form.
To fill out the continuing review form, researchers should provide updates on the study's progress, participant safety, any changes to the protocol, and expected duration of the study.
The purpose of the continuing review form is to evaluate the ongoing safety and efficacy of the research, ensuring that risks are minimized and that the study continues to comply with ethical standards.
The continuing review form must report information such as participant enrollment numbers, adverse events, changes to the research protocol, and any updates on informed consent processes.
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