COVID-19 Clinical Research Center | Informed Consent

Informed Consent Resources

  • IRB Form and Guidance
    Scroll approximately halfway down, and the following are under Forms and Instructions for COVID-19 Related Research:

    • Documentation Form for COVID-19 related Research Using an Oral Consent Process
    • Guidance for Informed Consent for COVID-19 Related Research
      Step-by-step instructions for consenting research participants for minimal risk and greater than minimal risk studies related to COVID-19


  • Witnessing COVID-19 Informed Consent

SOPs, special considerations, and resources for witnessing consent of COVID-19 research participants are available through the COVID-19 Informed Consent Pool on Microsoft Teams Contact to be added