Emergency Use Authorization

Lucira plans to expand the scope of the EUA next year. Pic: Lucira

FDA authorises first home self-testing kit for COVID-19

By Rachel Arthur

The U.S. Food and Drug Administration (FDA) has issued an emergency use authorization (EUA) for the Lucira COVID-19 All-In-One Test Kit: the first COVID-19 diagnostic test for self-testing at home.

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