As part of the updated EUA, REGEN-COV should be administered by intravenous (IV) infusion, with subcutaneous ... and who are at high risk for progression to severe COVID-19, ...

LONDON, Dec. 1, 2021 /PRNewswire/ -- LumiraDx (Nasdaq: LMDX) announced today that the intended use for its Food and Drug Administration (FDA) Emergency Use Authorization (EUA) SARS-CoV-2 RNA STAR ...

Aditxt's EUA submissions are for tests designed to, among other things: (i) reveal levels of antibodies neutralizing COVID-19; and (ii) quantify the level of antibodies that attack various targets ...

SAN DIEGO, June 15, 2020 /PRNewswire/ -- Agena Bioscience, a global provider of low cost and high-throughput molecular testing solutions, today announced the launch of the iPLEX® Pro SARS-CoV-2 ...

ChromaCode’s Emergency Use Authorization (EUA) is expanded by the FDA for its High-Throughput HDPCR™ SARS-CoV-2 Real-Time PCR assay ...

It means the EUA will not come before the presidential election. Full coverage of the coronavirus outbreak "We may know whether or not our vaccine is effective by the end of October," Bourla wrote.

May 21 (Reuters) - Vincent Medical Holdings Ltd: * GOT EUA FROM US FDA FOR INSPIREDTM O2FLO HIGH FLOW RESPIRATORY HUMIDIFIER & ACCESSORIES AND HYPNUSTM ST730 NON-INVASIVE VENTILATOR Source text ...