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26.11.2021 - QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced its polymerase chain reaction (PCR) tests remain accurate and effective in detecting SARS-CoV-2 infections in light of the emergence of a new variant of concern detected in ... Seite 1
FDA grants EUA to Qiagen’s digital SARS-CoV-2 antibody test 13 May 2021 (Last Updated May 13th, 2021 09:58) Qiagen’s portable rapid test has received FDA EUA for Covid-19 antibody detection. Share Article The test was found to have 93.85% sensitivity and 97.83% specificity. Credit: Qube’s Pictures from Pixabay. The US Food and Drug Administration (FDA) has granted emergency use authorisation (EUA) to Qiagen’s portable, rapid QIAreach Anti-SARS-CoV-2 Total Test for Covid-19 antibody detection. Developed in collaboration with Australian di...