Begin Application

Parts A, B, C, and D

General applicant information, research study synopsis, approval signatures, and summary of research proposal
    PDF Logo Application for the Use of Human Subjects
    PDF Logo Biosketch Form

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Part E

Consent documents, scripts for oral consents
    Word Logo Standard Consent Form
    Word Logo Implied Consent (Minimal Risk Surveys)
    Word Logo Consent Statement for Exempt Research
    Word Logo Focus Group Consent Language
    Word Logo Parental/Guardian Permission for a Minor
    Word Logo Child Assent 7-14
    Word Logo Youth Assent 15-17
    PDF Logo Request for Waiver or Modification of Consent


Part F

Any and all questionnaires, surveys, interview questions, discussion questions

For instructions on submitting qualtrics surveys, please see this instruction page.


Part G

Biosketches of all Research Personnel (each Biosketch should be no longer than 2 pages)
    PDF Logo Biosketch Form


Part H

Any and all other supporting documents (i.e. letters of support from other institutions/universities, grant applications, curriculum vitae)
    Word Logo Photo Release Form
    Word Logo Video Release Form
    Word Logo Institutional Approval
    Word Logo Telephone Survey Script


Adverse Event Report

Investigators are required to report Serious or Significant and Related to the Research Adverse Events to the Institutional Review Board for Human Subjects when discovered during the course of the research and/or no later than 5 days after their occurrence.
    Word Logo View Adverse Event Report form

Criteria for IRB Approval


This is only a cursory overview. Please familiarize yourself with the regulations:
45 CFR 46.111 (a)(1i) & (a)(2)