Business · 28/06/2021Updated: 10/17/2026 · 1 min read

FDA Determines Regulatory Review Period for Smallpox and Monkeypox Vaccine Extension

Summary

The US Food and Drug Administration has officially confirmed the review period for a patent extension application related to the Smallpox and Monkeypox Vaccine, Live, as required by law, following a submission to the US Patent and Trademark Office.

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

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