Business · 04/04/2011Updated: 10/17/2026 · 1 min read
FDA Announces Guidance on Emergency Research Exemptions from Informed Consent
Summary
The Food and Drug Administration (FDA) has released a guidance document to help institutions, investigators, and sponsors navigate the process of conducting emergency research without obtaining informed consent from participants, as allowed under specific FDA regulations.
Original source language: Federal Register — Health and Human ServicesOpen original release →