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Revised 020602 CONTINUING REVIEW REPORT OR COMPLETION REVIEW REPORT RESEARCH INVOLVING THE CARE AND USE OF ANIMALS SOUTHERN ILLINOIS UNIVERSITY EDWARDSVILLE (SIDE) (As required by the USDA, this form

How to fill out continuing review reportor completion

How to fill out continuing review report or completion:

1. Start by gathering all the necessary information and documents related to the study or project that is being reviewed. This may include research protocols, consent forms, participant enrollment numbers, adverse events reports, and any other relevant data.
2. Review the specific guidelines and requirements provided by the governing ethics committee or institutional review board (IRB) for completing the continuing review report or completion. Familiarize yourself with the format, sections, and any specific instructions that need to be followed.
3. Begin by completing the administrative information section of the report. This typically includes the name of the principal investigator, study or project title, study location, study sponsor, and other relevant details.
4. Provide a summary of the study progress so far. Include information on how many participants have been enrolled, any modifications made to the study protocol, and any safety concerns or adverse events that have occurred during the reporting period.
5. Describe any changes or updates made to the study protocol during the reporting period. This may include amendments to the informed consent process, modifications to the study design, or changes in the eligibility criteria for participants.
6. Discuss any challenges or difficulties encountered during the study, and how they were addressed. This could be related to recruitment, retention, data collection, or any other aspect of the research process.
7. Evaluate the ethical considerations and any potential risks or benefits associated with the study. Provide an assessment of whether the study is still meeting the requirements for participant safety and welfare.
8. Include any additional documentation or information requested by the ethics committee or IRB, such as progress reports, data analysis, or updates on financial disclosures.

Who needs continuing review report or completion?

1. Researchers conducting studies or projects that involve human participants and have received approval from an ethics committee or IRB.
2. Principal investigators who are responsible for overseeing the study and ensuring compliance with ethical guidelines and regulations.
3. Institutions, organizations, or research facilities that have policies in place for ongoing oversight and monitoring of research involving human participants.

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What is continuing review report or completion?

Continuing review report or completion refers to the process of periodically reviewing and updating a research study to ensure that it continues to meet ethical and regulatory requirements.

Who is required to file continuing review report or completion?

Researchers conducting studies that involve human subjects are required to file continuing review report or completion.

How to fill out continuing review report or completion?

To fill out continuing review report or completion, researchers need to provide updated information about the study protocol, informed consent documents, recruitment materials, and any adverse events that have occurred since the last review.

What is the purpose of continuing review report or completion?

The purpose of continuing review report or completion is to ensure that research involving human subjects remains ethically and scientifically sound throughout the course of the study.

What information must be reported on continuing review report or completion?

Information that must be reported on continuing review report or completion includes any changes to the study protocol, updated informed consent documents, recruitment materials, and any adverse events.