The approval of Pfizer COVID-19 vaccines for children under five years old hits another delay as the Food and Drug Administration (FDA) needed more data.
The U.S. Food and Drug Administration (FDA) advisory committee has revealed another side effect of Moderna's COVID-19 vaccine for those with cosmetic facial fillers.
American biotechnology company Moderna announced recently that they commit to distributing six million vaccines upon the emergency use authorization of the U.S. FDA.
The U.S. Food and Drug Administration (FDA) put the emergency use authorization for blood plasma as a COVID-19 Treatment on hold, reported The New York Times.
U.S. Food and Drug Administration has approved Roche, the Swiss drugmaker, for antibody tests that will determine whether people have ever been infected by COVID-19.
The United States Food and Drug Administration has announced its approval to use the COVID-19 testing kit that will give results or detections within 45 minutes.
