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.
How NPP Is Changing With the Onset of COVID-19
Artificial Intelligence, At-Home Testing, Behavioral Changes, Conferences, Coronavirus Disease (COVID-19) Pandemic, Digital, Doctors, Electronic Health Records, HCPs, Health Insurance, Healthcare Communications Agencies, Marketing & Advertising, Physicians, Sales Forces, Sales Reps, Social Media, Telemedicine, Trends, VeevaGreater Than One’s Christa Toole analyzes how healthcare marketers are adjusting to the current health crisis in a variety of ways.