1. U.S. Food and Drug Administration (FDA)-Regulated Research Routine Compliance Reviews
Office of Research Compliance
UW-4086
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2. UW–Madison Investigational New Drug/Investigational Device Exemption (IND/IDE) Registry
Office of Research Compliance
UW-4084
3. Institutional Review Board (IRB) Operations
Office of Research Compliance
UW-4144
4. Training for UW–Madison Investigators Who Hold an Investigational New Drug (IND) or Investigational Device Exemption (IDE)
Office of Research Compliance
UW-4085
5. Use of Human Fetal Tissue in Research
Office of Research Compliance
UW-4077
6. Human Research Protection Program (HRPP) Operations
Office of Research Compliance
UW-4143
7. Control of Test Articles Used in Research (Human Research Protection Program)
Office of Research Compliance
UW-4078
8. Principal Investigator Status for UW–Madison Studies Involving Human Participants
Office of Research Compliance
UW-4063
9. School of Medicine & Public Health – Consent for Sensitive Exams Under Anesthesia or Other Sedation
SMPH Office of Academic Affairs
SMPH-80100
10. Food and Drug Administration (FDA) Inspections and External Audits
Office of Research Compliance
UW-4083