Institutional Review Board Resources

Federal Regulations

Code of Federal Regulations (45 CFR 46)

Ethical Codes of Research Conduct

Belmont Report

Declaration of Helsinki

Nuremberg Code

Additional Websites

Office for Human Research Protections (OHRP)

National Institutes of Health (NIH) (Biomedical Research use)

Informed Consent

Informed Consent Guide

Informed Consent Checklist for Investigators

Guide for Writing Consent Forms

Adverse Events and Unanticipated Problems Reporting Form

All adverse events or unanticipated problems must be reported to the IRB office within one (1) business day of the occurrence or investigator's knowledge of the event.‌

Adverse Event and Unanticipated Problem Reporting Form

Office for Human Research Protections (OHRP)

OHRP Information for Participants 

Informed Consent

Information regarding the informed consent process can be found here.