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IRB Continuing Review Form Principal Investigator: Study Title: Study Status: Active Enrollment closed. Participants are receiving study treatment Enrollment closed. Participants are not receiving

How to fill out irb continuing review form

How to fill out irb continuing review form:

1. Begin by reviewing the instructions provided by your Institutional Review Board (IRB) for filling out the continuing review form. These instructions will typically outline the specific documents and information that need to be included in the form.
2. Gather all the necessary documents such as the previous IRB approval letter, any amendments or modifications made since the last review, and any other relevant supporting documentation.
3. Start by providing basic information about the study, such as the title, study ID number, and principal investigators' names and contact information.
4. Describe the progress of the study since the last review. Include details about the number of participants enrolled, any adverse events or issues encountered, and any changes made to the study protocol.
5. Explain any modifications made to the study since the last review. This can include changes to the study design, recruitment procedures, consent forms, or any other relevant aspects.
6. Provide a summary of the data collected thus far, including any preliminary findings or analysis conducted. This section should give an overview of the study's progress and any potential implications or insights gained from the data.
7. Discuss any challenges or issues encountered during the study and how they were addressed. This can include difficulties in recruitment, participant non-compliance, or unforeseen logistical issues.
8. Outline any changes or updates in the study team, including additions or departures of researchers or staff members involved in the project.
9. Detail any changes or updates to the study's funding sources, if applicable. This can include new grants received or changes in financial support for the study.
10. Finally, include any additional information or documentation required by your specific IRB for the continuing review form.

Who needs irb continuing review form:

1. Researchers conducting studies involving human subjects that have received initial IRB approval will typically need to submit an IRB continuing review form.
2. Institutions or organizations that have an IRB responsible for ensuring the protection of human subjects in research will require researchers to submit a continuing review form at specified intervals.
3. The IRB continuing review form is necessary to assess the progress, ethical considerations, and ongoing compliance of the study to ensure the protection and welfare of human subjects.

For pdfFiller’s FAQs

What is irb continuing review form?

The IRB continuing review form is a document used to update the Institutional Review Board (IRB) on the progress, safety, and ethical considerations of an ongoing research study.

Who is required to file irb continuing review form?

Researchers conducting studies that have been approved by the IRB are required to file the IRB continuing review form. This includes principal investigators, co-investigators, and any other individuals involved in the research process.

How to fill out irb continuing review form?

The IRB continuing review form should be completed by providing accurate and up-to-date information regarding the study's progress, any changes to the protocol, participant enrollment status, adverse events, and any other relevant updates. It is important to follow the instructions provided by the specific IRB or institution conducting the review.

What is the purpose of irb continuing review form?

The purpose of the IRB continuing review form is to ensure that ongoing research studies continue to meet ethical standards, participant safety is maintained, and any changes to the study protocol or procedures are reviewed and approved by the IRB before implementation.

What information must be reported on irb continuing review form?

The IRB continuing review form typically requires information such as the study title, principal investigator, study progress, participant enrollment status, any adverse events or complications, any changes to the study protocol, and any other relevant updates or concerns regarding the research study.

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