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Vela Diagnostics' ViroKey SARS-CoV-2 RT-PCR Test Receives the US FDA's Emergency Use Authorization

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Vela Diagnostics' ViroKey SARS-CoV-2 RT-PCR Test Receives the US FDA's Emergency Use Authorization

Shots:

  • The US FDA has granted EUA to the Vela’s PCR test that detects SARS-CoV-2 n nasopharyngeal and oropharyngeal swabs
  • The manual version of the ViroKey enables flexible sample processing and quick adoption of the test by laboratories with existing ABI 7500 Fast Dx instruments but for high throughput testing- an automated version of the assay is used for the optimization  of a workflow consisting of the Sentosa SX101 instrument- in conjunction with ABI 7500 Fast Dx PCR instrument or the Sentosa SA201 instrument
  • ViroKey SARS-CoV-2 RT-PCR Test has also received the CE mark and provisional approval from the Singapore Health Sciences Authority

­ Ref: Vela Diagnostic | Image: Biospectrum Asia

Click here to­ read the full press release 

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