Cue Health Gets FDA EUA for Monkeypox Molecular Test
The nucleic acid amplification test returns results in 25 minutes and is authorized for use in professional point-of-care settings.
Boston University, Cepheid Get FDA EUAs for COVID-19, Monkeypox Tests
The Cepheid test qualitatively detects DNA from monkeypox virus clade II and non-variola Orthopoxvirus in human lesion swab specimens.
DiaCarta Nabs FDA Emergency Use Authorization for Monkeypox Test
The laboratory-use QuantiVirus MPXV Test Kit targets two regions of the MPXV genome to detect the virus even if mutations occur in one target region.
Becton Dickinson Monkeypox PCR Assay Granted FDA Emergency Use Authorization
The PCR test is designed to qualitatively detect monkeypox virus DNA in human lesion swab samples from patients suspected of monkeypox infection.
Thermo Fisher Scientific Receives FDA Emergency Use Authorization for Monkeypox PCR Assay
The test is designed to qualitatively detect DNA from the monkeypox virus and screen for non-variola orthopoxviruses in human lesion swab samples.