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CONTINUING REVIEW FORM Title of Research: Approval Period: From To (NOTE: Any data collected before the approval date or after the end date shown above is not covered by IRB approval. If the project

How to fill out continuing review form

How to fill out a continuing review form:

1. Begin by carefully reviewing the instructions provided with the form. Make sure you understand the purpose and requirements of the continuing review process.
2. Collect all relevant documents and information that may be needed to complete the form. This may include previous research protocols, participant information, and any changes or updates that have occurred since the initial review.
3. Start filling out the form by providing basic information such as the title of the research project, the principal investigator's name, and contact details.
4. Proceed to answer the specific questions outlined in the form. Pay close attention to any instructions or guidelines provided for each question.
5. If there have been any changes or modifications to the original research protocol, document them clearly in the appropriate sections of the form. Additionally, describe any adverse events or unanticipated problems that have occurred during the study.
6. Include any updates on the recruitment and consent process, as well as the status of enrolled participants. Provide details on any measures taken to ensure the welfare and rights of the participants.
7. Review the completed form for accuracy and completeness. Make any necessary revisions or additions before finalizing the document.
8. Submit the completed continuing review form according to the specified instructions or submission process. Be sure to meet any deadlines and include all required supporting documents.
9. Following submission, monitor any communication or feedback from the review board. Address any concerns or requests for additional information promptly and thoroughly.

Who needs a continuing review form:

1. Researchers who are conducting ongoing studies involving human subjects typically need to complete a continuing review form.
2. This form ensures that the research project is continuously evaluated for ethical and regulatory compliance throughout its duration.
3. It is an essential requirement for maintaining the approval and validity of the research, allowing for the proper protection of participants and the ethical conduct of the study.
4. The need for a continuing review form may vary depending on the specific regulations and guidelines of the research institution or regulatory body overseeing the study.
5. Typically, researchers involved in clinical trials, longitudinal studies, or any research involving human subjects will need to complete and submit a continuing review form as part of the research compliance process.

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What is continuing review form?

The continuing review form is a document that researchers must submit to the Institutional Review Board (IRB) to provide an update on the progress of their research study.

Who is required to file continuing review form?

Researchers who are conducting a research study that has been approved by the IRB are required to file a continuing review form.

How to fill out continuing review form?

Researchers must provide information on the progress of the research study, any adverse events that have occurred, and any changes to the study protocol.

What is the purpose of continuing review form?

The purpose of the continuing review form is to ensure that the research study is being conducted in accordance with ethical guidelines and regulations.

What information must be reported on continuing review form?

Researchers must report on the progress of the research study, any adverse events, and any changes to the study protocol.