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Roche: EUA for cobas MPXV test in US

(CercleFinance.com) - Roche announces that the US FDA has granted an Emergency Use Authorization (EUA) for cobas MPXV, a real-time PCR assay for the qualitative detection of simian orthopoxvirosis virus DNA, for use on cobas 6800/8800 systems.


This high-throughput test for simian orthopoxvirosis virus (MPXV) becomes the first to receive an EUA following evaluation on real patient samples, rather than just laboratory-formulated samples.

High-throughput solutions enable rapid results, enabling individuals to avoid additional testing or unnecessary isolation, and facilitating access to appropriate treatment as soon as possible, the Swiss healthcare group said.


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