IRB Renewal Form

Section 1

Please enter the following information about yourself:
Today's date: Today's date: / MM / DD YYYY
Name: Name: First Last
Email:
Your Academic Program/Department/Office:
Your status (faculty, staff, graduate or undergraduate student):
Adviser or Faculty Sponsor (if applicable):
If you are a graduate or undergraduate student, has your Adviser or Faculty Sponsor seen and approved your renewal application?

If you are a graduate or undergraduate student, has your Adviser or Faculty Sponsor seen and approved your renewal application? Yes No
Your Adviser's or Faculty Sponsor's email address (if applicable):
Please list all individuals (full name and status, i.e., faculty, staff, student) involved in this project that will be working with human subjects. Note: Everyone listed must have completed Human Subject Research Training within the past three years.
If you have external funding for this research, provide the name of the sponsor(s) and associated project title(s).
Section 2

Please enter the following information about your project.
Case number of your previously approved IRB protocol.
Date of prior IRB approval: Date of prior IRB approval: / MM / DD YYYY
Have there been any changes in your research question, recruitment method, the target population, the research procedures, the consent process, and/or how you will secure the data?

Have there been any changes in your research question, recruitment method, the target population, the research procedures, the consent process, and/or how you will secure the data? Yes, there have been changes in my protocol No, there have been no changes in my protocol
If you answered "Yes" to the previous question, describe the change(s) in detail.
Have any research participants experienced any type of adverse event during the past year (events that caused unanticipated harm or distress) or have you received complaints from any participants about your research?

Have any research participants experienced any type of adverse event during the past year (events that caused unanticipated harm or distress) or have you received complaints from any participants about your research? Yes No
If you answered "Yes" to the previous question, describe in detail the adverse event and/or the complaint.
Section 3

To finalize and submit your application. Please verify that you have completed this form fully and accurately.
Finalize and Submit

If you have not already done so, you must ask your adviser to email a statement on your behalf to [email protected] The statement should read, "I have reviewed [your name]'s proposal and I will continue to oversee this research in its entirety."

Please read the following statement carefully:

I agree to obtain IRB approval prior to continueing my work with human subject participants. I will only perform the research as described in the above application; I will seek IRB approval of any proposed modifications in the approved study. I will inform the IRB if I receive any complaints from research participants within two days of receiving said compliant. I certify that all of the information contained in this proposal is accurate and truthful.

Submitting this form means that you affirm the statement above and will comply with the content. This counts as your legally binding signature.

IRB Renewal Form

IRB Renewal Form

Section 1

Section 2

Section 3

Finalize and Submit