BD, BioGX announce FDA Emergency Use Authorization submissions for new COVID-19 diagnostics for use in U.S.
FRANKLIN LAKES, N.J. — BD (Becton, Dickinson and Company) a leading global medical technology company, and BioGX, a molecular diagnostics company, announced that the companies have submitted Emergency Use Authorization requests to the U.S. Food and Drug Administration (FDA) for new diagnostic tests that, if authorized, would increase the potential capacity to screen for COVID-19 (coronavirus)
