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Regulation & law · 04/11/2022Updated: 10/17/2026 · 1 min read

CDC Redelегates Authority Under FD&C Act for Emergency Use Instructions

Summary

The Centers for Disease Control and Prevention (CDC) has transferred the authority to create and issue amended emergency use instructions (EUIs) to healthcare providers and individuals, allowing them to administer products for conditions that deviate from approved labeling and standard medical practice, from the Director of CDC to the Director of the National Center for Immunizations and Respiratory Diseases (NCIRD).

Original source language: Federal Register — All DocumentsOpen original release →

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