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Continuing Review Form1. 2. 3. 4. 5. To renew the study: Complete and send this report at least 30 days prior to the approval expiration date The PI or Designee must complete and sign this report
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How to fill out continuing review form

01
To fill out a continuing review form, follow these steps:
02
Begin by reviewing the instructions provided with the form to ensure you understand the requirements and purpose of the review.
03
Gather all relevant information and documents related to the study or research project that is being reviewed.
04
Start completing the form by providing basic information such as the title of the study, the name of the principal investigator, and the date of the original approval.
05
Proceed to answer the specific questions or sections of the form regarding the progress of the study, any modifications made since the last review, and any adverse events or issues encountered.
06
If applicable, include any updated consent forms, recruitment materials, or study protocols that have been revised.
07
Ensure that all sections of the form are completed accurately and thoroughly, providing explanations or additional information as necessary.
08
Review the completed form to verify that all responses are clear, consistent, and in compliance with the relevant regulations and guidelines.
09
Obtain any required signatures from the principal investigator, co-investigators, or other authorized individuals.
10
Submit the completed form and any supporting documents to the appropriate ethics committee or institutional review board (IRB).
11
Keep a copy of the completed form and supporting documents for your records.

Who needs continuing review form?

01
The continuing review form is typically required for individuals or organizations conducting research or studies involving human subjects.
02
Institutional review boards (IRBs), ethics committees, or regulatory authorities may request the submission of a continuing review form to ensure ongoing compliance with ethical standards and regulatory requirements.
03
Principal investigators, co-investigators, or researchers responsible for the oversight and management of the study or research project may need to complete this form.
04
It is important to consult the specific regulations, guidelines, or policies applicable to your jurisdiction or institution to determine if a continuing review form is required for your particular study or research project.
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The continuing review form is a document that researchers must submit to the Institutional Review Board (IRB) to request approval for the continuation of a research study.
Researchers conducting a study that has been approved by the IRB are required to file a continuing review form to request approval for the continuation of the study.
To fill out the continuing review form, researchers must provide updated information on the study protocol, any adverse events, changes in study personnel, and any new information that may affect the risk-benefit ratio of the study.
The purpose of the continuing review form is to ensure that the study is still in compliance with ethical guidelines, regulations, and the original study protocol.
The continuing review form must include updates on the study protocol, any adverse events, changes in study personnel, and any new information that may affect the risk-benefit ratio of the study.
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