www.fdanews.com/articles/197207-quidels-covid-19-test-receives-emergency-use-authorization
Quidel’s COVID-19 Test Receives Emergency Use Authorization
May 20, 2020
Quidel has received a new EUA from the FDA for its Lyra Direct SARS-CoV-2 assay.
The updated test replaces upfront RNA sample extraction with a 10-minute heat step to cut processing time by up to 50 minutes.
The assay can run on polymerase chain reaction machines made by Applied Biosystems, Bio-Rad, Qiagen, Roche and Thermo Fisher.