WASHINGTON — Pfizer and BioNTech announced Monday that they have submitted an application to the U.S. Food and Drug Administration for emergency use authorization of a booster dose of their bivalent ...

Pfizer Inc applied to U.S. health regulators on Friday for emergency use authorization (EUA) of its COVID-19 vaccine, the first such application in a major step toward providing protection against the ...

Pfizer and BioNTech said a third booster shot is believed to raise Omicron-fighting antibodies by 36 times Pfizer and BioNTech announced on Tuesday they have submitted an application to the U.S. Food ...

Manufacturing is underway and doses of Moderna's Spikevax 2024-2025 formula will be ready to ship as early as August, pending regulatory approval The most common solicited local adverse event for ...

Pfizer said Monday that it has submitted its application to the Food and Drug Administration (FDA) for an updated COVID-19 vaccine targeting the omicron subvariant currently circulating. The ...

Europe's drugs watchdog said on Thursday it expects to receive the first application for conditional marketing approval for a COVID-19 vaccine "in the coming days", the latest step towards making a ...

Co-Diagnostics withdrew its 510(k) application for its COVID-19 test to submit an enhanced version addressing shelf-life stability concerns. The new submission will incorporate platform improvements, ...

FORT WAYNE, Ind.--(BUSINESS WIRE)--Enterprise Health, an occupational and employee health IT solution provider, today launched Channel 19, a stand-alone application to help employers and hospital ...

This study observed a rapid increase in the integration of telehealth- and COVID-19–related apps with electronic health records during the COVID-19 pandemic. Objectives: To (1) track the integration ...