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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 FormDOC
IRB Applications Forms
IRB Protocol Application for New Projects (NEW 2019)DOC
Existing Human Subjects Data FormDOC
Course Umbrella Protocol Application for Class Projects DOC
IRB Course Protocol ChecklistDOC
IRB Supplemental Forms
Continuing Review Form (NEW 2019)DOC
Research Personnel Addition FormPDF
Modification FormDOC
Closure FormDOC
Adverse Event FormDOC
Unanticipated Problem FormDOC
Participant Concern or Complaint FormPDF
Noncompliance Report FormPDF
Non-English Speaking Participants FormDOC
Public Data Set Nomination FormDOC
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 TemplateDOC
Example Debriefing Script for Deception StudyPDF
DNP Site Permission TemplateDOC
Research Review Categories
Exempt Research Categories (NEW 2019)DOC
Expedited Review Research Categories (Non-Exempt)DOC
Reference Documents
IRB Identifiers ChartPDF
HIPAA Quick Reference GuideDOC
International Human Subjects Research Regulations Link
E.U. Guidance General Data Protection Directive (GDPR)Link
Amazon Mechanical Turk: IRB ConsiderationsPDF

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

IRB Registration:I0RG0004550 
Federal Wide Assurance:FWA00011478 

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

IRB Registration:I0RG0004550 
Federal Wide Assurance:FWA00011478 

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 FormDOC
IRB Applications Forms
IRB Protocol Application for New Projects (NEW 2019)DOC
Existing Human Subjects Data FormDOC
Course Umbrella Protocol Application for Class Projects DOC
IRB Course Protocol ChecklistDOC
IRB Supplemental Forms
Continuing Review Form (NEW 2019)DOC
Research Personnel Addition FormPDF
Modification FormDOC
Closure FormDOC
Adverse Event FormDOC
Unanticipated Problem FormDOC
Participant Concern or Complaint FormPDF
Noncompliance Report FormPDF
Non-English Speaking Participants FormDOC
Public Data Set Nomination FormDOC
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 TemplateDOC
Example Debriefing Script for Deception StudyPDF
DNP Site Permission TemplateDOC
Research Review Categories
Exempt Research Categories (NEW 2019)DOC
Expedited Review Research Categories (Non-Exempt)DOC
Reference Documents
IRB Identifiers ChartPDF
HIPAA Quick Reference GuideDOC
International Human Subjects Research Regulations Link
E.U. Guidance General Data Protection Directive (GDPR)Link
Amazon Mechanical Turk: IRB ConsiderationsPDF