Emergency Use Authorization

Emergency Use Authorization Recent News

Roche's Cobas COVID Test Scores EUA For Asymptomatic People
What's Going On With Novavax Stock?
Novavax, Inc (NASDAQ: NVAX) shares fell over 12% in the after-hours trading on Monday after closing almost 8.8% lower in regular trading.
Pfizer-BioNTech COVID-19 Vaccine Gets FDA Emergency Approval For Age Group 12-15
The U.S. Food and Drug Administration on Monday approved the emergency use of Pfizer Inc. (NYSE: PFE) and BioNTech SE’s (NASDAQ: BNTX) COVID-19 vaccine in adolescents aged between 12 to 15 years.
Why Ocugen Shares Skyrocketed Today
Ocugen Inc (NASDAQ: OCGN) shares soared 42.9% in the regular session and another 11% in the after-hours session on Thursday.
OraSure Files Emergency Use Application For COVID-19 Kits For Home Use And Professional Test
OraSure Technologies Inc (NASDAQ: OSUR) 
FDA Updates Fact Sheets For Eli Lilly, Regeneron's COVID-19 Antibody Therapies Under Emergency Use
The FDA updat
Johnson & Johnson Seeks US Emergency Approval For Single Dose COVID-19 Vaccine
Johnson & Johnson (NYSE: JNJ) said Wednesday that its subsidiary Janssen Biotech Inc is requesting approval from the United States Food and Drug Administration for its single-dose COVID-19 vaccine candidate.
Moderna COVID-19 Vaccine Secures FDA Panel's Approval
Moderna Inc's (NASDAQ: MRNA) COVID-19 vaccine has received the go-ahead from an advisory panel of the U.S. Food and Drug Administration, paving the way for the company to secure an emergency use authorization (EUA).
Pfizer COVID-19 Vaccine Could Get Emergency Approval By Friday, FDA Advisor Says
A member of a United States Food and Drug Administration committee on vaccines said that the agency could issue an emergency authorization for Pfizer Inc’s (NYSE: PFE) COVID-19 vaccine as early as Friday.
Eli Lilly's Arthritis Drug Gets Emergency Use Approval For Treatment Of COVID-19
Eli Lilly And Co’s (NYSE: LLY) rheumatoid arthritis drug baricitinib has been issued an emergency use authorization, in combination with Gilead Sciences, Inc’s (NASDAQ: GILD) remdesivir, for the treatment of CO
Pfizer Expected To File For FDA Emergency Approval on Friday, Followed Closely By Moderna, Azar Says
Pfizer Inc (NYSE: PFE) is likely to file an application with the United States Food and Drug Administration for emergency use of its COVID-19 vaccine on Friday, with Moderna Inc (NASDAQ: MRNA) to do the same shortly after.
No Conclusive Evidence On Convalescent Plasma Use Against COVID-19, NIH Says After FDA Emergency Use Approval
The National Institutes Of Health said Tuesday that after reviewing available evidence from published and unpublished data on convalescent plasma therapy for COVID-19, it had concluded there is no case for recommending or advising against such a treatment.
Roche To Launch Rapid COVID-19 Test In Europe This Month, Seek FDA Emergency Use Approval
Roche Holding AG (OTC: RHHBY) said Tuesday it will launch a COVID-19 rapid antigen test in late September in Europe and intends to file for emergency use authorization (EUA) in the United States.
Abbott Gets FDA Emergency Use Approval For $5 Rapid COVID-19 Test
The United States Food and Drug Administration granted emergency use authorization to a 15-minute COVID-19 test produced by Abbott Laboratories (NYSE: ABT) on Wednesday.
Quest Gets FDA Emergency Approval For New Lab Method To Improve Coronavirus Testing Capacity, Speed
Quest Diagnostics Inc (NYSE: DGX) announced Wednesday it had received an emergency use authorization from the Food and Drug Administration for a new laboratory technique that can help signficantly expand and speed up novel coronavirus (COVID-19) testing.