Requirements for your IRB Application
- Determine your level of review
- Description of Project and Procedures
- Consent Form and/or assent script
- Human Research Protection Training Certificate
- All measures, questionnaires, and/or interview questions
- Debriefing letter/script (if deception is used)
- Wording or advertisements for recruitment on social media, email, or paper flyers (if applicable)
Preview the application before you begin for reference: IRB Application
Determine Your Level of Review
Before you can submit an Institutional Review Board Application, you will need to determine your level of review (risk).
- Level I: Exempt (no foreseeable risk)
- Level II: Expedited Review (minimal risk)
- Level III: Full Board Review (more than minimal risk and protected subjects)
This information is required for your IRB Application. Please take a moment to carefully consider the checklist worksheet and follow the corresponding instructions.
Complete your Human Research Protection Training
- A copy of the certifications of completion from the following online training program must be submitted to the IRB.
- You will need to complete Human Research Protection Training (Lessons 1-5) and submit your certificates for each lesson.
Create Informed Consent Material
Informed consent is the cornerstone of ethical human subjects research. There are specific requirements for consent material to meet the criteria of "Informed Consent." The video below presents the Informed Consent process from the perspective of the participant. Keep these points in mind when you create your informed consent material.
Informed Consent for Research: What to Expect video
Templates for Informed Consent
What MUST be included in Informed Consent Material?
- What is the name of the project? Who is the Principal Investigator/Student Investigators.?
- Describe the purpose of the research in under 100 words. If the project is a class project include the class name and number.
- Describe what the participant will do in under 100 words.
- How will you record the information? How will you store and secure the information? How long will you store the information?
- What are the risks to the participant?
- What are the benefits to the participant?
- Is there any compensation for participating? If there is compensation/benefit, what are the alternatives?
- Will the data you collect be used for other research?
- Are the data collected anonymously? How will you maintain confidentiality?
- Information about withdrawal from the study.
- Who does the participant contact if they have concerns or questions (Faculty PI/Sponsor and IRB email addresses)?
Complete you IRB Application
Once you have gathered all of the materials required above, you may fill in your application.
Institutional Review Board Application
IRB Recertification
Approval of a human subject research proposal is good for one year, unless the project has acceptable but potential risk in which case approval is given for a six-month period. If the project will continue beyond the approval period, principal investigators are required to resubmit documents for review prior to the expiration date of the initial approval.