Responding to increased public and congressional criticism of its arguably too-flexible approach to regulatory oversight of serological tests used to detect COVID-19 antibodies, on May 4, 2020, the ...

The FDA has just published a list of certain already-on-the-market serology/antibody tests from commercial manufacturers that should not be distributed unless and until an Emergency Use Authorization ...

A new serological test can not only help humanity prepare for and respond to the next pandemic, but it also can be pivotal in the search for viral triggers of diseases like diabetes and celiac disease ...

Children with coronavirus disease 2019 (COVID-19), or those who have been infected with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), may have prolonged symptoms such as headache, ...

FDA recently authorized the first COVID-19 serology test that detects neutralizing antibodies from recent or prior SARS-CoV-2 infection. The emergency use authorization went to biotechnology company ...

Please provide your email address to receive an email when new articles are posted on . In its recent guidance on serology and antibody testing for SARS-CoV-2, the American Association for Clinical ...

Eurobio Scientific (FR0013240934, ALERS, eligible PEA-PME), a leading French group in the field of specialty in vitro medical diagnostics, and NG Biotech, a French biotechnology company specializing ...