Expedited or Full Board Review

• New Protocol Application: Social/Behavioral/Educational Research
• New Protocol Application: Biomedical Research
• Application for Continuing Review/Renewal of IRB Protocol
• Application for Modifications to an Approved IRB Protocol

Exempt Protocol Review

• Application for Exempt Protocol Determination

Informed Consent Templates

• Informed Consent For Participation in Research Study:
  Social/Behavioral/Educational Research
• Informed Consent For Participation in Research Study:  
  Biomedical Research
• Assent Form - Minors Participating in a Research Study
• Parental Permission for Minor Participating in Research Study
• Information Sheet - Consent For Research Participation (Exempt Research Studies only)
• Authorization to Disclose Protected Health Information (PHI) for Research Purposes

Appendices 

• Appendix P - Use of Protected Health Information
• Appendix V-B Vulnerable Population - Pregnant Persons Neonates Fetuses
• Appendix V-C Vulnerable Population - Prisoners
• Appendix V-D Vulnerable Population - Children
• Appendix W - Waivers Regarding Informed Consent Process
• Appendix T - Tissue and Biological Sample Use
• Appendix F1  FDA-Drug
• Appendix F2  FDA-Devices
• Appendix E:  Electronic Data Security

Collaborative Studies (IRB and Investigator Agreements)

• Individual Investigator Agreement RFU
• IRB Authorization Agreement1 RFUMS as IRB of record
• IRB Authorization Agreement 2 RFUMS Not the IRB of record
• SMART IRB (single IRB application from relying institution)

Other Forms

• Post-Approval Problem Report Form
• Scientific Validity Assessment Form
• Addition or Deletion to Research Team 
• Voluntary Closure of IRB Protocol Form
• Supplement:  Progress Report Form (only for 7 Year de novo Applications)
• Not Human Research (NHR) Guidance and Determination Form (includes QA_QI)