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Continuing Review Form A completed Continuing Review form must be submitted in hard copy to the Director of Institutional Research (Esquivel roan estate.edu) for all research continuing beyond the

How to fill out continuing review form

How to fill out a continuing review form?

1. Review the form: Start by carefully reviewing the continuing review form to understand its format and the information it requires. Familiarize yourself with the sections and questions included in the form.
2. Gather necessary documentation: Collect any supporting documents or information that may be required to complete the form. This may include previous study protocols, participant consent forms, adverse event reports, and any other relevant documents.
3. Provide study details: Begin by filling out the necessary study details, such as the study title, principal investigator's name, study start and end dates, and the IRB (Institutional Review Board) protocol number. Ensure accuracy when entering this information.
4. Update participant information: Provide an update on participant information—this may include the number of participants currently enrolled, any newly recruited participants, and any withdrawn participants. If applicable, provide details regarding any changes in participant eligibility criteria.
5. Assess study progress: Review the study's progress and indicate the status of the research. Specify whether the study is ongoing, completed, or terminated. If the study is ongoing, inform the IRB if any modifications have been made to the study protocol.
6. Report adverse events and side effects: If any adverse events or side effects have occurred during the study period, provide a comprehensive summary of these incidents. Describe the actions taken to address these events and any measures implemented to prevent future occurrences.
7. Update conflicts of interest: Disclose any conflicts of interest that may have arisen since the last review. This includes any financial relationships, professional affiliations, or personal interests that may influence the study.
8. Renew approval: If your study requires continuation beyond the current review period, clearly state the duration for which you are seeking approval. Indicate whether any modifications or amendments to the study protocol have been submitted along with the continuing review form.
9. Submit the form: Once you have completed all the required sections of the continuing review form, ensure that all the information provided is accurate and up to date. Sign and date the form before submitting it to the appropriate IRB or ethics committee.

Who needs a continuing review form?

Researchers conducting studies involving human participants or animal subjects often need to complete a continuing review form. This form is typically required by the IRB or ethics committee responsible for overseeing the research to ensure that it continues to meet ethical standards and remains compliant with regulations. Continuing review forms are necessary to assess the progress of ongoing studies, identify any potential risks to participants, review any modifications made to the study protocol, and determine if the study should be allowed to continue. Researchers and principal investigators are usually responsible for completing the continuing review form and submitting it to the IRB for evaluation and approval.

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What is continuing review form?

Continuing review form is a document submitted to the Institutional Review Board (IRB) to provide an update on the progress of a research study and ensure compliance.

Who is required to file continuing review form?

Researchers conducting studies involving human subjects are required to file a continuing review form.

How to fill out continuing review form?

Continuing review forms can typically be filled out online or through a specific submission portal provided by the IRB. Researchers must provide updates on the study progress, any adverse events, and any protocol modifications.

What is the purpose of continuing review form?

The purpose of the continuing review form is to ensure that the research study is still ethical, safe, and compliant with regulations. It allows the IRB to monitor the progress of the study and make any necessary adjustments.

What information must be reported on continuing review form?

Researchers must report on the progress of the study, any adverse events, any changes to the study protocol, and any new information that may impact the safety of the participants.