Biotech Values

[DewDiligence]

ABT’s COVID-19 IgG test receives FDA EUA:

In FDA’s continuing effort to increase the availability of serology – i.e. antibody – tests, we issued an emergency use authorization (EUA) to Abbott Laboratories Inc. for its SARS-CoV-2 IgG serology test. This is FDA’s eighth EUA for a serology test. https://t.co/PjWkgj2R2Q pic.twitter.com/u6henGBRNl

— Dr. Stephen M. Hahn (@SteveFDA) April 27, 2020