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What does IRB require?

The Regulations IRB review and approval is required for projects that: Meet the definition of research. Involve human subjects and. Include any interaction or intervention with human subjects or involve access to identifiable private information.

How do I complete the IRB process?

A Step-by-Step Guide for IRB Submissions Step 1: Human participant research training. Step 2: Project design. Step 3: Your IRB protocol: form choice, completion, and submission. Step 4: IRB evaluation of your protocol. Step 5: Post-approval activities.

How do I prepare for an IRB submission?

To prepare for a submission to the IRB, the investigator must generally develop a protocol (not required for studies that meet the criteria for exemption), any relevant consent form(s), recruitment materials (written or printed in alternative media, as applicable), and complete the IRBs electronic application in eIRB.

What is the IRB application form?

The IRB application is used to provide information to the IRB whose responsibility it is to ensure the university adheres to federal regulations in the protection of human participants in research. No recruitment or data can be collected until an application is approved by the IRB.

What materials need IRB approval?

All materials aimed at recruiting participants into a research study (including the final copy of printed advertisements, scripts, audio or video tapes, or web sites) must be reviewed and approved by the IRB prior to use (HRP-315).

What documents are needed for IRB submission?

IRB Submission Checklist Spelling and grammar have been checked and are correct. Signed Application (Principal Investigator, Faculty Sponsor) All supporting documents arranged in the following order: Application. Consent Document(s) Recruitment Materials. Study Instrument(s) Permission Letters (if applicable)

What information must be included in the research proposal that is submitted to the IRB?

The research proposal describes the protocol you will follow and can include: the research hypothesis, study background, design and methodology, data analysis, study procedures, details about the subject population, inclusion/exclusion criteria, recruitment, informed consent process, benefits, risks, privacy and

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