Research Ethics & Compliance

Templates & Forms

Investigators preparing IRB submissions use these templates for protocols and consent documents. Additional IRB templates are provided to promote transparency of IRB operations. Forms are used by IRB staff, members, and investigators as a reference or tool for IRB submissions.

Templates

• Protocol Writing
  • HRP-503 – TEMPLATE PROTOCOL – Biomedical Research
  • HRP-503a – TEMPLATE SBS PROTOCOL – Social/Behavioral Research
  • HRP-503b – UA human-subjects-research-determination-form
  • HRP-503c – UA Quality Improvement-Quality Assurance-determination-form
  • HRP-503d – TEMPLATE – Developmental Approval
• Informed Consent
  • HRP-502 – TEMPLATE CONSENT DOCUMENT
  • HRP-506 – TEMPLATE CONSENT DOCUMENT – Expanded Access
  • HRP-507 – TEMPLATE CONSENT DOCUMENT – Short Form 
• Multisite Research
  • HRP-508 – TEMPLATE – SITE SUPPLEMENT
• Other
  • HRP-504 – TEMPLATE LETTER – School Permission to Conduct Research

Forms

• Multisite
  • HRP-811 – FORM – Basic Site Information
  • HRP-813 – FORM – Site Modification
  • HRP-815 – FORM – Institutional Profile
  • HRP-816 – FORM – External IRB Study Update
• Incident Reporting
  • HRP-214 – FORM – Reportable New Information
  • HRP-814 – FORM – Site Reportable New Information
• Continuing Review
  • HRP-812 – FORM – Site Continuing Review
• IRB and HRPP Review Documents
  • HRP-202 – FORM – IRB Member Information