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QIAGEN (QGEN) and DiaSorin said Monday that the U.S. Food and Drug Administration has approved the LIAISON QuantiFERON-TB Gold Plus assay for use on DiaSorin's automated LIAISON XS platform.


RTTNews | Nov 29, 2021 01:25AM EST

01:24 Monday, November 29, 2021 (RTTNews.com) - QIAGEN (QGEN) and DiaSorin said Monday that the U.S. Food and Drug Administration has approved the LIAISON QuantiFERON-TB Gold Plus assay for use on DiaSorin's automated LIAISON XS platform.

The company noted that the approval widens the accessibility of U.S. customers to automation solutions for processing QIAGEN's blood-based test for latent tuberculosis (TB) detection and support the conversion from the traditional tuberculin skin tests that were developed over a century ago.

LIAISON QuantiFERON-TB Gold Plus is an interferon-gamma release assay (IGRA) developed by QIAGEN and DiaSorin to offer streamlined laboratory automation for latent TB screening.

QuantiFERON-TB - which tests for interferon-gamma released from T-cells that have encountered TB bacteria - has been available on LIAISON XL platforms in the U.S. since 2019.

Read the original article on RTTNews ( https://www.rttnews.com/3245167/qiagen-says-fda-approves-quantiferon-tb-gold-plus-assay-on-liaison-xs-platform.aspx)

For comments and feedback: contact editorial@rttnews.com

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