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QIAGEN N.V. QGEN recently secured FDA clearance for the QIAstat-Dx Respiratory Panel Plus syndromic test. Previously authorized under the FDA Emergency Use Authorization (âEUAâ) as the QIAstat-Dx Respiratory SARS-CoV-2 Panel, the test is designed to support clinical decision-making in diagnosing upper respiratory infections and covers 21 viral and bacterial targets.
The latest development will strongly boost the companyâs Molecular Diagnostics business.
Significance of the QIAst...
>>> Read more: QIAGEN (QGEN) Wins FDA Nod for QIAstat-Dx Respiratory Panel Plus
The latest development will strongly boost the companyâs Molecular Diagnostics business.
Significance of the QIAst...
>>> Read more: QIAGEN (QGEN) Wins FDA Nod for QIAstat-Dx Respiratory Panel Plus