TBG Biotechnology Obtained US FDA Emergency Use Authorisation for ExProbeTM SARS-CoV-2 Testing Kit

  • Jun 14, 2020 AEST
  • Team Kalkine


TBG Diagnostics Limited (ASX:TDL) announced that its 100% owned subsidiary TBG Biotechnology Corp received an  Emergency Use Authorisation from the US Food and Drug Administration for its ExProbeTM SARS-CoV-2 Testing Kit.

ExProbeTM is an RNA based diagnostic kit that uses real time PCR technology with multiplex model to detect distinctive segments within RdRP, N and E genes of the SARS-CoV-2 virus in a single reaction.

The US Food and Drug Administration has made this kit available under an emergency access mechanism known as EUA for the detection and/or diagnosis of COVID-19.





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