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DiaSorin C. diff test gets FDA approval

March 15, 2017DiaSorin received clearance from the Food and Drug Administration to market its Simplexa C. difficile Direct assay.

The assay, first launched outside of the U.S. in late 2016, was developed by DiaSorin Molecular to be run on the Liaison MDX. It is a scalable benchtop instrument able to provide real-time PCR results for quantitative, qualitative, multianalyte, and sample-to-answer detection needs.

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