Review of FDA-Regulated Research Policy
Summary: This policy applies to how the Minimal Risk and Health Sciences IRBs apply US Food and Drug Administration (FDA) regulations to human subjects research.
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Applicable HRPP Policy
- Control of Test Articles Used in Research Policy
- Clinical Trials Registration & Results Reporting
- Emergency Use of Test Articles and of Humanitarian Use Devices Policy
- Exempt Research
- Humanitarian Use Device Policy
Attachments and Other References