IRB Forms

Please refer to SOP #1: Determining if IRB Review is Required for guidance on whether your project will require IRB approval.

IRB Forms and Resources
COVID-19 and Human Subjects Research
COVID-19 Guidance for Human Subjects Research
COVID-19 Safety Plan for Resuming Existing In-Person Studies
COVID-19 Information Packet for In-Person Participants
Determining if IRB Review is Required
Determination of Human Subjects Research Form
IRB Decision Tree
IRB Application Forms
IRB Protocol Application for New Projects (Updated Sept 2020)
Existing Human Subjects Data Form
IRB Course Umbrella Protocol Form for Class Projects
IRB Course Protocol Checklist for Student Projects
IRB Supplemental Forms
IRB Continuing Review Form (New 2019)
IRB Modification Request Form
IRB Research Personnel Change Form
IRB Closure Form
IRB Unanticipated Problem Report Form
Participant Concern or Complaint Form
IRB Noncompliance Report Form
Non-English Speaking Participants Form
IRB Public Data Set Nomination Form
IRB Consent Templates and Checklist
Informed Consent Template (NEW 2019)
Parental Consent Template
Assent Template for Minors (NEW 2019)
Information Sheet Template (NEW 2020)
Informed Consent Checklist (NEW 2019)
IRB Sample Templates
DNP Site Permission Template
Debriefing Script for Studies Involving Deception Template
Sample IRB Recruitment Flyer
IRB Reference Documents
IRB Identifiers Guidance
HIPAA Quick Reference Guide
International Human Subjects Research Regulations
E.U. Guidance General Data Protection Regulations (GDPR)
Amazon MTurk: IRB Considerations (Source: Stanford University)

IRB Chair

Anca Miron

mirona@uwosh.edu

IRB Administrator
Kelly Schill
(920) 424-3375
IRB@uwosh.edu

Office located in Dempsey Hall Suite 214

IRB Registration:I0RG0004550
Federal Wide Assurance:FWA00011478

IRB Chair

Anca Miron

mirona@uwosh.edu

IRB Administrator
Kelly Schill
(920) 424-3375
IRB@uwosh.edu

Office located in Dempsey Hall Suite 214

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 and Resources
COVID-19 and Human Subjects Research
COVID-19 Guidance for Human Subjects Research
COVID-19 Safety Plan for Resuming Existing In-Person Studies
COVID-19 Information Packet for In-Person Participants
Determining if IRB Review is Required
Determination of Human Subjects Research Form
IRB Decision Tree
IRB Application Forms
IRB Protocol Application for New Projects (Updated Sept 2020)
Existing Human Subjects Data Form
IRB Course Umbrella Protocol Form for Class Projects
IRB Course Protocol Checklist for Student Projects
IRB Supplemental Forms
IRB Continuing Review Form (New 2019)
IRB Modification Request Form
IRB Research Personnel Change Form
IRB Closure Form
IRB Unanticipated Problem Report Form
Participant Concern or Complaint Form
IRB Noncompliance Report Form
Non-English Speaking Participants Form
IRB Public Data Set Nomination Form
IRB Consent Templates and Checklist
Informed Consent Template (NEW 2019)
Parental Consent Template
Assent Template for Minors (NEW 2019)
Information Sheet Template (NEW 2020)
Informed Consent Checklist (NEW 2019)
IRB Sample Templates
DNP Site Permission Template
Debriefing Script for Studies Involving Deception Template
Sample IRB Recruitment Flyer
IRB Reference Documents
IRB Identifiers Guidance
HIPAA Quick Reference Guide
International Human Subjects Research Regulations
E.U. Guidance General Data Protection Regulations (GDPR)
Amazon MTurk: IRB Considerations (Source: Stanford University)