Please refer to SOP #1: Determining if IRB Review is Required for guidance on whether your project will require IRB approval.
| IRB | Forms |
|---|---|
| Determining if IRB Review is Required | |
| Determination of Human Subjects Research Form | DOC |
| IRB Applications Forms | |
| IRB Protocol Application for New Projects (NEW 2019) | DOC |
| Existing Human Subjects Data Form | DOC |
| Course Umbrella Protocol Application for Class Projects | DOC |
| IRB Course Protocol Checklist | DOC |
| IRB Supplemental Forms | |
| Continuing Review Form (NEW 2019) | DOC |
| Research Personnel Addition Form | |
| Modification Form | DOC |
| Closure Form | DOC |
| Adverse Event Form | DOC |
| Unanticipated Problem Form | DOC |
| Participant Concern or Complaint Form | |
| Noncompliance Report Form | |
| Non-English Speaking Participants Form | DOC |
| Public Data Set Nomination Form | DOC |
| IRB Consent Templates and Checklist | |
| Informed Consent Template (NEW 2019) | DOC |
| Assent Template (NEW 2019) | DOC |
| Informed Consent- Additional Template Language for Special Circumstances (NEW 2019) | Coming Soon |
| Informed Consent Checklist (NEW 2019) | DOC |
| Additional IRB Sample Templates | |
| Example IRB Recruitment Flyer Template | DOC |
| Example Debriefing Script for Deception Study | |
| DNP Site Permission Template | DOC |
| Research Review Categories | |
| Exempt Research Categories (NEW 2019) | DOC |
| Expedited Review Research Categories (Non-Exempt) | DOC |
| Reference Documents | |
| IRB Identifiers Chart | |
| HIPAA Quick Reference Guide | DOC |
| International Human Subjects Research Regulations | Link |
| E.U. Guidance General Data Protection Directive (GDPR) | Link |
| Amazon Mechanical Turk: IRB Considerations |
Contact IRB
2019-2020 Interim IRB Chair
Melissa Bublitz
bublitzm@uwosh.edu
IRB Administrator
Kelly Schill
(920) 424-3375
IRB Administration
(920) 424-3215
irb@uwosh.edu
Office located in Dempsey Hall Suite 214
IRB Quick Look
Contact IRB
2019-2020 Interim IRB Chair
Melissa Bublitz
bublitzm@uwosh.edu
IRB Administrator
Kelly Schill
(920) 424-3375
IRB Administration
(920) 424-3215
irb@uwosh.edu
Office located in Dempsey Hall Suite 214
IRB Quick Look
Please refer to SOP #1: Determining if IRB Review is Required for guidance on whether your project will require IRB approval.
| IRB | Forms |
|---|---|
| Determining if IRB Review is Required | |
| Determination of Human Subjects Research Form | DOC |
| IRB Applications Forms | |
| IRB Protocol Application for New Projects (NEW 2019) | DOC |
| Existing Human Subjects Data Form | DOC |
| Course Umbrella Protocol Application for Class Projects | DOC |
| IRB Course Protocol Checklist | DOC |
| IRB Supplemental Forms | |
| Continuing Review Form (NEW 2019) | DOC |
| Research Personnel Addition Form | |
| Modification Form | DOC |
| Closure Form | DOC |
| Adverse Event Form | DOC |
| Unanticipated Problem Form | DOC |
| Participant Concern or Complaint Form | |
| Noncompliance Report Form | |
| Non-English Speaking Participants Form | DOC |
| Public Data Set Nomination Form | DOC |
| IRB Consent Templates and Checklist | |
| Informed Consent Template (NEW 2019) | DOC |
| Assent Template (NEW 2019) | DOC |
| Informed Consent- Additional Template Language for Special Circumstances (NEW 2019) | Coming Soon |
| Informed Consent Checklist (NEW 2019) | DOC |
| Additional IRB Sample Templates | |
| Example IRB Recruitment Flyer Template | DOC |
| Example Debriefing Script for Deception Study | |
| DNP Site Permission Template | DOC |
| Research Review Categories | |
| Exempt Research Categories (NEW 2019) | DOC |
| Expedited Review Research Categories (Non-Exempt) | DOC |
| Reference Documents | |
| IRB Identifiers Chart | |
| HIPAA Quick Reference Guide | DOC |
| International Human Subjects Research Regulations | Link |
| E.U. Guidance General Data Protection Directive (GDPR) | Link |
| Amazon Mechanical Turk: IRB Considerations |