Right Here. Wright State. This Fall.

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Policies, Procedures, and Forms

Please note that updates and news can now be found on the IRB General Information page.

Frequently Used Supplemental Forms

Researcher Education,Training, Credentialing Requirements

IRB Operations

Human Subject Research Submission and Review

Informed Consent

Research HIPAA/Protected Health Information (PHI)

Reportable Events, Non-Compliance and Reporting

Research Involving Investigational Drugs

Research Involving Devices

Emergency Use - Drugs, Devices, Biologics

Please review Emergency Use requirements on page 6 of P21 Research Involving Medical Devices linked above.

Reliance on an External IRBs

ClinicalTrials.gov