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This form is required for non-exempt studies that need ongoing evaluation by the North Texas Regional Institutional Review Board (NTR IRB). Investigators must complete, sign, and submit the form in IRBNet while ensuring all questions are answered completely to avoid delays in the review process.
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How to fill out ntr irb continuing review

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How to fill out ntr irb continuing review

01
Gather all necessary study materials and documents related to your research.
02
Review your original IRB approval and any previous continuing review submissions.
03
Complete the NTR IRB Continuing Review Form with accurate and updated information.
04
Provide a summary of the research progress and any changes since the last review.
05
Include any adverse events or changes in risks to participants.
06
Submit any amended documents if changes have been made to the research protocol.
07
Ensure that all required signatures are collected before submission.
08
Submit the completed form by the designated deadline as instructed by the IRB.

Who needs ntr irb continuing review?

01
Researchers who have ongoing projects that were previously approved by the NTR IRB and need to continue the research beyond the initial approval period.
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NTR IRB continuing review is a process conducted by an Institutional Review Board (IRB) to assess the ongoing ethical conduct of research studies that involve human subjects. It ensures that the study continues to comply with ethical standards, regulations, and the initial approval obtained from the IRB.
Researchers who are conducting studies that were approved by the IRB and are still ongoing are required to file for NTR IRB continuing review, typically those responsible for the conduct of the research.
To fill out the NTR IRB continuing review, researchers must complete a specific form provided by the IRB, detailing the progress of the study, any changes to the protocol, new information affecting risk assessment, and an update on the participant recruitment and data collection status.
The purpose of NTR IRB continuing review is to monitor the ethical and safety aspects of ongoing research to ensure that the rights and welfare of participants are being protected throughout the study duration.
Information that must be reported includes any unanticipated problems involving risks to participants, changes to the study protocol, recruitment progress, new safety information, and an overall assessment of risks versus benefits.
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