Get the free Continuing Review / Interim Report of Human Subjects Research

Questions regarding IRRB submissions can be directed to 330 344-6947 or by emailing IRRB akrongeneral.org. I agree to comply with all applicable AGMC policies and procedures and applicable federal state and local laws. Have there been any changes in the consent/assent process since the last IRRB review Yes No N/a For studies still enrolling please attach the most recent consent/assent document s. FOR IRRB USE ONLY IRRB Number IRRB Reviewer Exempt Expedited Full Institutional Research...

How to fill out continuing review interim report

How to fill out continuing review interim report

1. Start by gathering all the necessary documents and information required for the continuing review interim report.
2. Review the previous review report and make note of any changes or updates that need to be included in the new report.
3. Clearly state the purpose of the continuing review interim report at the beginning.
4. Provide a brief summary of the research project and the progress made since the last review.
5. Include any changes to the study design, recruitment methods, or participant population, if applicable.
6. Report any adverse events or concerns that have occurred during the study period.
7. Provide updated information on the research team, including any new personnel or changes in roles.
8. Include a detailed description of any modifications made to the informed consent process or materials.
9. Clearly state any potential risks or benefits associated with the continued participation of the participants in the study.
10. Conclude the report by summarizing the overall progress and any recommendations for further action or improvements.
11. Review and revise the draft report before final submission to ensure accuracy and clarity.

Who needs continuing review interim report?

1. Continuing review interim report is typically required by institutional review boards (IRBs) or ethics committees overseeing research studies.
2. Researchers conducting studies involving human participants or animal subjects may need to submit a continuing review interim report.
3. Institutional policies and regulations may vary, so it is important to check the specific requirements of the governing body or organization.

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What is continuing review interim report?

Continuing review interim report is a document that provides an update on the progress of an ongoing research study that has been approved by an Institutional Review Board (IRB).

Who is required to file continuing review interim report?

Researchers and principal investigators conducting approved research studies are required to file continuing review interim report as per the regulations of the IRB.

How to fill out continuing review interim report?

Continuing review interim report can be filled out by providing details on the progress of the research study, any changes made to the study protocol, and any adverse events that have occurred during the study period.

What is the purpose of continuing review interim report?

The purpose of continuing review interim report is to ensure that the research study is being conducted in compliance with ethical guidelines, regulations, and the approved protocol.

What information must be reported on continuing review interim report?

Information that must be reported on continuing review interim report includes the progress of the study, any amendments made to the study protocol, any adverse events, and any deviations from the approved protocol.