FDA to Issue Emergency Use Authorization for Monkeypox Tests
In a move to expand access to lab testing for monkeypox, HHS has authorized the FDA to issue EUAs for in vitro diagnostic tests for the virus.
In a move to expand access to lab testing for monkeypox, HHS has authorized the FDA to issue EUAs for in vitro diagnostic tests for the virus.
In July, ICATT took a major step toward equitable access to testing by enlisting two of the country’s leading COVID-19 PCR test providers.
With the final rule on PT published July 11, here are the five things lab managers need to know to keep their labs compliant.
Centers for Disease Control and Prevention spearheads US effort to quickly increase lab testing capacity and access.
Recent FDA Safety Communication warns of the potential of false results from other sample types when testing for the monkeypox virus.