Shots: The FDA has issued a EUA for Simoa Semi-Quantitative SARS-CoV-2 IgG Ab test and can be operated on Simoa HD-X Analyzer The test checks for Abs that are directed […]readmore
Tags : Emergency Use Authorization
Shots: The EUA is based on ACCT-2 study assessing baricitinib (4mg, qd for 14 days or until hospital discharge) in combination with remdesivir vs PBO with remdesivir in hospitalized patients […]readmore
Shots: The US FDA has granted EUA to the Vela’s PCR test that detects SARS-CoV-2 n nasopharyngeal and oropharyngeal swabs The manual version of the ViroKey enables flexible sample processing […]readmore
Shots: Abbott’s SARS-CoV-2 IgG lab-based serology blood test is the fourth COVID-19 detection test to receive the FDA’ EUA based on Alinity i platforms, which is a next-generation immunoassay instrument […]readmore
Shots: The US FDA has granted EUA for its COVID-19 Droplet Digital PCR (ddPCR) test that runs on Bio-Rad’s QX200 and QXDx ddPCR systems Due to its high sensitivity, the […]readmore
Shots: Roche has received the US FDA’s EUA for its Elecsys anti-SARS-CoV-2 Ab test to detect patient’s immune response to the COVID-19 and run on its cobas e analysers, delivering […]readmore
Shots: The EUA is based on two global P-III studies assessing 5-day & 10-day dosing durations of remdesivir (IV) vs PBO in patients with mod. to sev. symptoms of COVID-19, […]readmore
Shots: Shots: The company receives EUA for its Novodiag COVID-19 molecular diagnostic test used to detect SARS-CoV-2 virus rapidly and is now available in Finland and under process for obtaining […]readmore
Shots: The EUA allows nasal swab specimens to be collected at home using Pixel by LabCorp COVID-19 test home collection kit if recommended by HCPs following the completion of the […]readmore
Shots: The US FDA has granted EUA to Ortho’s total Ab assay for COVID-19, the VITROS immunodiagnostic products Anti-SARS-CoV-2 total reagent pack and calibrators and is considered as one of […]readmore