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FDA-cleared PCR test aids in the faster identification of three distinct conditions within an hour SUNNYVALE, Calif., Nov. 15, 2022 /PRNewswire/ -- Cepheid announced today that it has launched Xpert... | November 15, 2022
BioGX previously helped develop a monkeypox and orthopoxvirus assay on the GeneXpert that was validated on clinical samples in 2017.
/PRNewswire/ -- Cepheid today announced it has received the CE mark for Xpert® Xpress CoV-2 plus, a rapid molecular diagnostic test for qualitative detection...
New "plus" version of test adds a 3rd gene target to enhance detection of future SARS-CoV-2 variants SUNNYVALE, Calif., May 19, 2022 /PRNewswire/ -- Cepheid today announced it has received
/PRNewswire/ -- Cepheid today announced it has received Emergency Use Authorization (EUA) from the U.S. Food & Drug Administration (FDA) for Xpert® Xpress...