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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Feb. 3, 2017

View Archived Issues

FDA adds whole blood Zika detection to Abbott's emergency use authorization

The U.S. Food and Drug Administration has given its first nod to a molecular test developed by Abbott Laboratories for the Zika virus for use to test whole blood. This expands upon an existing use of the test from the Abbott Park, Ill., company; it had already received emergency use authorization for use to test serum, plasma and urine. Read More

India's national budget leaves domestic med techs frustrated

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India's CDSCO delays due date for device final rule to January 2018

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First commercial Reactiv8 system from Mainstay sold and implanted in Germany

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Guardant to make liquid biopsy standard of care with MD Anderson partnership

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Appointments and advancements

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Financings

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Product briefs

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Regulatory front

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Other news to note

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MDD's Diagnostics Extra

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