New coronavirus test 10 times faster is FDA approved

Roche Holding AG won emergency approval from the U.S. government for a highly automated coronavirus test, potentially speeding up tenfold the ability to test patients.

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The U.S. Food and Drug Administration granted an “emergency use authorization” to the test, which runs on Roche’s cobas 6800/8800 systems. The tool also is available in Europe and countries that accept its CE marking for medical devices, Roche said.

The 8800 version is capable of testing 4,128 patients a day, and the 6800 can test as many as 1,440, the Basel, Switzerland-based company said.

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