The FDA has amended its Emergency Use Authorization for Quidel’s (OTC:QDEL)
rapid point-of-care Sofia SARS Antigen FIA test to allow it to be run
on its automated Sofia Fluorescent Immunoassay Analyzer that can
generate results in as little as 15 minutes.
https://seekingalpha.com/news/3581808-fda-oks-expanded-emergency-use-of-quidel-covidminus-19-test
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