Federal Register website news: The US Food and Drug Administration announced the revocation of the emergency use authorization granted to Pfizer for Pfizer's Lucilla COVID-19 and influenza household testing products.

Zhitongcaijing · 12/31/2025 13:57
Federal Register website news: The US Food and Drug Administration announced the revocation of the emergency use authorization granted to Pfizer for Pfizer's Lucilla COVID-19 and influenza household testing products.