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Business · 27/03/2018Updated: 10/17/2026 · 1 min read

FDA Releases Draft Guidance on Elemental Impurities in Animal Drug Products

Summary

The Food and Drug Administration (FDA) has published a draft guidance for industry (GFI) #255, addressing changes in the USP requirements for controlling elemental impurities in animal drug products marketed in the US

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

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