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Business · 24/11/2003Updated: 10/17/2026 · 1 min read

FDA Announces Guidance on User Fees and Refunds for Premarket Approval Applications

Summary

The Food and Drug Administration (FDA) has released a new guidance document outlining user fees and refunds for premarket approval applications, including supplements and other submissions, and how these fees may be partially refunded.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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