The U.S. Food and Drug Administration authorized emergency use of the first over-the-counter Covid-19 antigen test, which can be used at home.

The U.S. Food and Drug Administration issued a new template for clinical test developers that is designed to assist these companies in developing and submitting emergency use authorization (EUA) for Covid-19 tests that can be performed at home or in other settings besides laboratories.

Greater Than One’s Christa Toole analyzes how healthcare marketers are adjusting to the current health crisis in a variety of ways.