- New Study Submissions to the IRB
- Submitting Requests for Exemption and Expedited Review to the IRB
- Submitting Continuing Reviews and/or Amendments to the IRB
- Informed Consent: Human Subjects Protections and Research Operation
- More on Consent: Translation, Non-English Speaking Subjects, Types of ICFs (Addendum, Tissue Banking, Genetic Research) and Waiver of Consent
- Inspections and Study Monitoring
- IRB Review of Study Advertisements
Future topics:
- Data and Safety Monitoring
- Emergency Use Exemption
- Pediatric Research, including Neonates
- Adverse Event Reporting
- International Research
- Research with Investigational Drugs
- Vulnerable Populations
The IRB office is available to present, or coordinate, a research education session for your Division or Department. Please call the office for more information, or to request a “Friday Education Session” topic.
