If you need assistance with protocol development, please contact our Research Navigator at firstname.lastname@example.org or 269.337.6471. If you have any IRB-related questions, please call our helpline at 269.337.4345.
- Protocol Templates
- Informed Consent Templates
- Exempt Human Research Consent Script Template
- Abbreviated Consent Form (with Signature Line)
- Recruitment Script Template (Example Language for Recruitment Scripts)
- Research Participant Information Sheet Template
- Consent to Participate in Online Research Study Template
- Social Behavioral Informed Consent Template
- Biomedical Informed Consent Template (with HIPAA Authorization)
- Case Report Informed Consent Template
All active studies have been transitioned to the new electronic system. Any changes to existing human research will be made via iMedRIS the new electronic system. If you are having any issues accessing the system and/or locating your study, please call the Office of the IRB at 269-337-4345.