FDA Approves Ebola Treatment
On December 21, the U.S. Food and Drug Administration approved Ebanga (Ansuvimab-zykl), a human monoclonal antibody, for the treatment of ebola (zaire ebolavirus) infection in…
On December 21, the U.S. Food and Drug Administration approved Ebanga (Ansuvimab-zykl), a human monoclonal antibody, for the treatment of ebola (zaire ebolavirus) infection in…
On December 18, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the second vaccine for the prevention of coronavirus disease…
On December 17, The U.S. Food and Drug Administration reported that nearly 50 male enhancement or weight loss products that have been found to contain…
Recently, on December 17, Centers for Disease Control and Prevention (CDC), published a report in collaboration with the Food and Drug Administration (FDA), in which…
On December 15, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the first over-the-counter (OTC) fully at-home diagnostic test for…
On December 11 the U.S. Food and Drug Administration issued the first emergency use authorization (EUA) for COVID-19 vaccine for the prevention of coronavirus disease…
On December 10 FDA (Food and Drug Administration) holds an advisory committee meeting to discuss authorization of COVID-19 vaccine candidate (vaccine from Pfizer and Biontech)…
Recently, The U.S. Food and Drug Administration (FDA) posted online background material for this week’s upcoming Vaccines and Related Biological Products Advisory Committee (VRBPAC) public…
On December 4, the U.S. Food and Drug Administration (FDA) announced about authorization of the first diagnostic test for at home collection of patient samples…
During the global outbreak of respiratory disease caused by a novel coronavirus that has been named “severe acute respiratory syndrome coronavirus 2” (SARS-CoV-2), appears treatments…