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Forms and Policies

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IRB Policies

IRB Forms

Adverse Event Forms

  • Adverse Event Reporting
  • Adverse Event Reporting Guidelines

Application Forms: Initial and Renewal

  • IRB-ITHS Application
  • IRB Application: Research Using Existing and Confidential Data, Records or Specimens
  • Application for Exempt Review Status
  • IRB Status Report
  • IRB Status Report: Research Using Existing and Confidential Data, Records or Specimens
  • Compassionate Use Device Form
  • Assent Form Template
  • Consent Form Template
  • Consent Form and Assent Form Checklists for Researchers
  • Short Form: Consent for Use with Language Minorities (Limited or Non-English Speaking Families)
  • Emergency Use Consent Form Template

HIPAA Related Forms

  • HIPAA Authorization: Permission to Use, Create and Share Health Information for Research
  • Research Disclosure Tracking

Patient Data Request Forms

  • HIM Patient Data Request
  • Research Chart Pull Request

Other Forms

  • Incident Report Form
  • Modification Request Form
  • Memo of Understanding Concerning Children's IRB Review Fees
  • IRB Criteria and Considerations
  • Optional Protocol Templates
  • Research Participants' Rights
  • Request for Tissue for Use in Research

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