Submission Applications and Other Forms

Human Research Protections Program

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I am extremely pleased with the IRB/HRPP process. It was smooth, thoughtful, and efficient. I felt adequately supported at every step along the way. 

Meg Warren (she/her)
Associate Professor, Management

HRPP NOTES

Processing Timeline Update

  • With a significant uptick in recent submissions, turnaround times are running slightly longer than those printed in the application and posted to the website. (Review Categories and Timelines indicate approximate turnaround schedules during normal times.)

IMPORTANT SUBMISSION INFORMATION: Always download the most recent HRPP submission forms and HRPP Consent and other templates when preparing a new submission. (Don't re-use previous application forms.)

Special Circumstances

IMPORTANT

You must have a written HRPP determination or approval before starting any project (including recruitment) that collects data from or about living individuals (except for publicly available data). Federal regulations prohibit retroactive determinations.

Initial Submission Forms

NOTE: Use only current submission forms. [Applications with outdated forms will be returned without processing.]

  • Application for Exemption/NHPR ~ Updated Nov. 2025
  • Expedited/Full-Board Application Form ~ Updated Sept. 2025.

Consult Review Categories and Timelines to determine the appropriate form for your project and for approximate turnaround timelines. Contact the HRPP with questions.

To avoid processing delays, closely follow all application submission instructions.

Post-Approval Protocol Management Forms

Use for required actions related to ongoing, approved protocols. For more information on researcher responsibilities and necessary actions depending on review-level, read the guidance on Protocol Management