QIAGEN to Resubmit QIAreach SARS-CoV-2 Antigen Test in Q1

 QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced that it plans to resubmit in the first quarter of 2021 its QIAreach SARS-CoV-2 Antigen Test to the U.S. Food and Drug Administration for Emergency Use Authorization to detect SARS-CoV-2 antigens in people with active infections in 15 minutes.

This comes after QIAGEN decided to proactively withdraw the first submission made in November 2020 for this product to address a chemistry-related issue. QIAGEN believes it has resolved the issue, and data is now being collected for submission to the FDA. The eHub used to read out test results is not affected.

“We are working closely with the FDA to ensure that all necessary information is submitted as quickly as possible so that we can make this product available as a solution in the fight against the COVID-19 pandemic, as many U.S. customers have expressed significant interest in using QIAreach to expand their testing capacity,” said Thierry Bernard, Chief Executive Officer of QIAGEN.

https://www.biospace.com/article/releases/qiagen-plans-to-resubmit-eua-submission-in-the-u-s-for-qiareach-sars-cov-2-antigen-test-in-the-first-quarter-of-2021/