US FDA Updates Template For OTC COVID-19 Test Development

The US FDA’s most recent update is intended to help test makers provide validation data and other information to the agency for developing at-home diagnostic tests.

Woman Taking At Home Test
• Source: Alamy

The US Food and Drug Administration updated a template used to help developers provide the necessary data and information in support of a pre-emergency use authorization (EUA) submission for OTC home-use molecular or antigen diagnostic COVID-19 tests.

The “Molecular and Antigen Home Use Test Template” now includes “updated recommendations and additional clarity for test developers,” the...

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