Get Irb Protocol Review Form - Auburn University

The IRB protocol review form is essential for researchers at Auburn University seeking to renew their research involving human subjects. This guide will help you navigate the form, ensuring that you complete each section accurately and efficiently while adhering to university guidelines.

Follow the steps to effectively fill out the IRB protocol review form.

1. Use the ‘Get Form’ button to access the IRB protocol review form and open it in your preferred editor.
2. Begin by entering the protocol number in the designated field, followed by the original IRB approval dates, specifying both the start and end dates.
3. Indicate the requested one-year maximum renewal period by filling out both the start and end dates.
4. Provide the project title in the space provided, making sure to be as descriptive as possible.
5. Complete the principal investigator section by entering your name, signature, and details such as your faculty advisor, title, department, and contact information.
6. Identify the current external funding agency associated with your project in the specified field.
7. List any contractors, subcontractors, or other entities or IRBs involved in your project as requested.
8. Briefly describe the activities that occurred over the past year that involved participants, using either a numbered or bulleted list.
9. Explain the rationale for requesting additional time to complete your research project.
10. Indicate whether you plan to make changes to your protocol if the renewal is approved by selecting 'Yes' or 'No', and if 'Yes', mention that a modification form is needed.
11. In the participant information section, provide the number of participants who took part in the research and any adverse events, unexpected difficulties, or benefits.
12. Note how many participants withdrew from the study and how many new participants you plan to recruit during the renewal period.
13. If you intend to re-contact participants, denote your plans and ensure you complete any required modification forms if not previously approved.
14. Address data protection by confirming if data is collected and stored as approved, and identify any changes in key research personnel with corresponding compliance proof.
15. Provide the anticipated date for the destruction of identifiable data and mention if it is not applicable.
16. Attach copies of all previously approved IRB documents and any new consent documents or information letters you will be using.
17. After completing the form, remember to submit a hard copy with all necessary signatures to the Office of Human Subjects Research at Auburn University.

Complete your IRB protocol review form online to ensure compliance and facilitate your research.