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Therma Bright Inc : Therma Bright Awaits FDA-EUA Approval From Over 260 AcuVid Clinical Study Test Results

Therma Bright Inc : Therma Bright Awaits FDA-EUA Approval From Over 260 AcuVid Clinical Study Test Results
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Premier Medical Corporation s COVID-19 Antigen Test to Seek Emergency Use Authorization in the U S

Share this article Share this article SOMERSET, N.J., April 7, 2021 /PRNewswire/ Premier Medical Corporation (PMC) – a leading manufacturer of COVID-19 Antigen and Antibody tests – plans to submit its COVID-19 Antigen rapid test for U.S. approval this month. PMC is submitting the Sure Status COVID-19 Antigen Card Test to the Food and Drug Administration (FDA) for inclusion in the Emergency Use Authorization program for distribution and use in the U.S. This comes after the test was included by the World Health Organization (WHO) in its Emergency Use Listing worldwide. Premier Medical Corporation is just the third company in the world, and the only Indian-based company, to accomplish this feat.

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