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TBRIF / Therma Bright provides update on US FDA application for its AcuVid COVID-19 rapid antigen saliva test

Therma Bright provides update on US FDA application for its AcuVid COVID-19 rapid antigen saliva test
Therma Bright Inc (TSX-V:THRM, OTC:TBRIF) said it has submitted follow-up answers and reformatted data to the US Food and Drug Administration (FDA) for the company's Emergency Use Authorization (EUA) application for its AcuVid COVID-19 Rapid Antigen Saliva Test. The Toronto-based company said its executive and product development teams have been working with FDA officials to clarify answers to some of the EUA application questions, as well as provided some reformatting of data to better meet the application template requirements. Read More
Posted: Jun 2 2022, 08:44
Author Name: Proactive Investors
Views: 111094

TBRIF News  

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