The student news site of The Harker School.

Harker Aquila

The student news site of The Harker School.

Harker Aquila

The student news site of The Harker School.

Harker Aquila

The U.S. Centers for Disease Control and Prevention (CDC) developed a test kit in February, during the early stages of the outbreak, but it proved to be faulty. As a result, the Food and Drug Administration (FDA) announced in March that it would begin to issue Emergency Use Authorizations (EUA) to clinical laboratories and commercial manufacturers that have produced tests that are screened by the FDA before their distribution and use.

COVID-19 testing and treatments explained: Cases ramp up as researchers race to find sustainable cures

by Mark Hu, Katie Wang, and Nicholas Wei May 20, 2020

As COVID-19 infections continue to spread across the nation, hospitals across Santa Clara Valley are taking measures to increase the number of resources available for patients, including ventilators and...

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