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Use for both continuing review and final report to close a protocol. If modifications are being requested, also submit and required documents. IRB Number: Protocol Name: Principal Investigator Name,
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Form continuing review progress is a document that tracks the ongoing review of a research study to ensure compliance with regulatory requirements and ethical standards.
Principal investigators and research teams conducting studies involving human subjects are required to file form continuing review progress.
Form continuing review progress can be filled out by providing detailed information about the study's progress, any changes made to the protocol, and any adverse events that have occurred.
The purpose of form continuing review progress is to ensure that research studies involving human subjects are being conducted ethically and in compliance with regulations.
Information such as recruitment status, protocol modifications, adverse events, and any new information that may impact the safety of participants must be reported on form continuing review progress.
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