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Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions.
Negative results must be combined with clinical observations, patient history, and epidemiological information.
This test was developed by Roche on COBAS® 6800/8800 and its performance characteristics verified by Poplar Healthcare. Cobas®
SARS-CoV-2 test is FDA approved under Emergency Use Authorization (EUA). Poplar Healthcare is regulated under CLIA as qualified
to perform high-complexity testing.