Fall 2022 IRB Presentations


Fall 2022 IRB presentations will be virtual, by Zoom. Please register to receive the Zoom link.

Checklists and Guidance Documents Galore!

The Human Subjects Office (HSO) offers a variety of checklists and documents that we hope the research community will use for various types of circumstances and scenarios. In this lecture, HSO staff will provide an overview of the following checklists and when to use them:

  • Exemption Tool – about the eight categories of research that qualify for Exempt Status
  • Two Informed Consent Document checklists – for biomedical research and social/behavioral researchers to make sure consent documents are consistent with the HawkIRB application
  • ClinicalTrials.gov checklist (NEW!) – incorporates all previous ClinicalTrials.gov and Applicable Clinical Trial (ACT) checklists
  • Investigational New Drug (IND) or Investigational Device Exemption (IDS) Checklists – about the reporting and record keeping responsibilities of researchers who hold an IND or IDE with the Food and Drug Administration (FDA)
  • FDA Site Inspection Guide – for when the FDA comes to inspect a study
  • Course Related Student Project Checklist – for student projects conducted as a course assignment
  • PI Departure Checklists – for the Human Research Protection Program and for funded research (external or internal funding)
Wednesday, October 5, 2022
9:00 AM - 10:30 AM
Zoom

Pre-registration is recommended.

Human Subjects Research Hot Topics & Updates – October 2022

Learn about new initiatives, HawkIRB enhancements (rolled out or in-production) and important information/reminders from the Institutional Review Board (IRB) and the UI Human Research Protection Program (HRPP). To supplement the information provided in the monthly IRB Connection Newsletter, the Human Subjects Office (HSO) offers these presentations at least three times a year to disseminate information in a timely manner and to be transparent about current projects and initiatives. Attendees will gain knowledge and resources necessary to design research projects, prepare thorough HawkIRB applications and effectively oversee the conduct of human subjects research.

Target audience:

  • Principal Investigators (PIs)
  • Faculty Advisors for student PIs
  • Study Coordinators
  • IRB Liaisons
  • Departmental Research Administrators
  • Others involved in human subjects research administration or oversight

The topics will be announced closer to the date of the presentation.

Wednesday, October 19, 2022
12:00 PM - 1:00 PM
Zoom

Pre-registration is recommended.