Close Menu

NEW YORK ─ The US Food and Drug Administration on Thursday granted Emergency Use Authorization to life science reagent company Zymo Research for its Quick SARS-CoV-2 rRT-PCR Kit for the detection of SARS-CoV-2 coronavirus.

The molecular kit, developed by the Irvine, California-based firm, has been authorized as a laboratory test for the detection of nucleic acid from SARS-CoV-2 in upper and lower respiratory specimens from patients suspected of COVID-19, the agency said.

To read the full story....

...and receive Daily News bulletins.

Already have a 360Dx or GenomeWeb account?
Login Now.

Don't have a 360Dx or GenomeWeb account?
Register for Free.