Business · 18/10/2002Updated: 10/17/2026 · 1 min read

FDA Announces Draft Guidance for Industry on Use of Human Blood and Blood Components

Summary

The FDA has released a draft document outlining acceptable practices for the use of human blood and blood components, which will help manufacturers comply with FDA regulations and label their products correctly.

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

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