If you need assistance with protocol development, please contact our Research Navigator at patrice.mason@med.wmich.edu or 269.337.6471. If you have any IRB-related questions, please call our helpline at 269.337.4345. All forms can now be accessed via the WMed IRB electronic system.
- Protocol Templates
- Informed Consent
- Recruitment Script Template (Example Language for Recruitment Scripts)
- Abbreviated Consent Form (Template for Most Non-Exempt, Low-Risk Studies - Interviews, Surveys, Focus Groups, etc.)
- Research Participant Information Sheet Template
- Consent to Participate in Online Research Study Template
- Social Behavioral Informed Consent Template
- Biomedical Informed Consent Template
- Request for Waiver of Consent
- Request for Waiver or Alteration of HIPAA Authorization
- IRB Member Forms
- Human Subjects Research Determination Checklist
- Initial Review
- HUD-Initial Review
- Exemption Determination
- Continuing Review-Convened Review
- Continuing Review-Expedited Review
- Continuing Review-HUD Event Reporting Form
- Elements of Consent Review
- Modification Review-Expedited
- Modification Review-Full Board