Resource: FDA Issues Emergency Use Authorization for First COVID-19 Vaccine
Source: U.S. Food and Drug Administration
Synopsis: The FDA issued the first emergency use authorization (EUA) for a vaccine

Resource: FDA Authorizes First Direct-to-Consumer COVID-19 Test System
Source: U.S. Food and Drug Administration
Synopsis: FDA authorized LabCorp’s Pixel COVID-19 Test Home Collection Kit for use by

Resource: COVID-19 and Flu Combination Test for use with home-collected samples
Source: U.S. Food and Drug Administration
Synopsis: FDA authorized the first diagnostic test for at home collection of

Resource: FDA Announces Advisory Committee Meeting to Discuss COVID-19 Vaccine Candidate
Source: U.S. Food and Drug Administration
Synopsis: The U.S. Food and Drug Administration has scheduled a

Resource: FDA Authorizes Monoclonal Antibodies for Treatment of COVID-19
Source: U.S. Food and Drug Administration
Synopsis: The FDA approved emergency use authorization for two antibody treatments to

Resource: FDA Authorizes The First At-Home Coronavirus Test
Source: New York Times
Synopsis: The Food and Drug Administration on Tuesday gave an emergency green light to the first rapid coronavirus

Resource: The FDA Grants Emergency Approval to Eli Lilly’s Antibody Treatment
Source: New York Times
Synopsis: The Food and Drug Administration has granted emergency authorization of a COVID-19

Resource: Pfizer’s COVID-19 Vaccine Proves 90% Effective in Latest Trials
Source: Wall Street Journal
Synopsis: A coronavirus vaccine developed by Pfizer Inc. and partner BioNTech SE showed in an

Resource: FDA COVID-19 Updates
Source: U.S. Food and Drug Administration
Synopsis: 

• The FDA updated guidance on the use of COVID-19 convalescent plasma. This extends the treatment. Through the

Resource: FDA Approves First Treatment for COVID-19
Source: U.S. Food and Drug Administration
Synopsis: FDA approved the antiviral drug Veklury (Remdesivir) for use in adult and pediatric patients 12