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INSTITUTIONAL REVIEW BOARD (IRB) CONTINUING REVIEW FORM FOR NONEXEMPT STUDIES Federal law requires that all nonexempt research projects approved by the IRB be monitored annually. Please complete this
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How to fill out continuing review form for

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To fill out a continuing review form, follow these steps:
02
Start by reading the instructions provided with the form. These instructions will guide you through the process and help you understand the purpose of the form.
03
Review the form carefully and ensure that you have all the necessary information and documents before you begin. This may include details about the research project, any changes made since the initial review, and any potential risks or benefits.
04
Fill in the required information, such as the title of the research study, the principal investigator's name, and the date of the review.
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Answer the questions on the form accurately and honestly. Provide any additional details or explanations as needed.
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Attach any relevant supporting documents or materials, such as updated consent forms or participant information sheets.
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Double-check your entries and make sure everything is correct and complete.
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Submit the completed form to the appropriate review board or committee according to their preferred method.
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Who needs continuing review form for?

01
The continuing review form is typically required for individuals or organizations involved in research projects that involve human subjects.
02
Researchers, principal investigators, and research institutions are often responsible for submitting the continuing review form to the appropriate review board or committee.
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This form helps ensure that ongoing research is conducted ethically, complies with relevant regulations and guidelines, and protects the rights and welfare of human subjects involved in the study.
04
The specific requirements for completing and submitting the continuing review form may vary depending on the institution, jurisdiction, and nature of the research study.

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Continuing review form is used to ensure the ongoing compliance of a research study with ethical standards and regulatory requirements.
Researchers conducting human subjects research are required to file a continuing review form.
Continuing review form should be filled out accurately and completely, including any updates to the study protocol, informed consent documents, and any other relevant information.
The purpose of a continuing review form is to assess the ongoing compliance of a research study and ensure the protection of human subjects.
Information such as any changes to the study protocol, adverse events, recruitment methods, and any other relevant updates must be reported on the continuing review form.
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