Business · 27/10/2010Updated: 10/17/2026 · 1 min read
FDA Announces Approval of Draft Guidance on Emergency Use Authorization of Medical Products
Summary
The Food and Drug Administration (FDA) has received approval from the Office of Management and Budget (OMB) for a collection of information related to a draft guidance on emergency use authorization of medical products, as required by the Paperwork Reduction Act of 1995.
Original source language: Federal Register — Health and Human ServicesOpen original release →