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Business · 24/02/20121 min read

FDA Releases Guidance on Adverse Event Reporting During Influenza Pandemic

The Food and Drug Administration (FDA) has published a guidance document outlining its approach to enforcing adverse event reporting requirements for medical products and dietary supplements during an influenza pandemic, focusing on reports related to flu prevention and treatment products.

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

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