New Jersey pharmaceutical firm Becton, Dickinson and Company has won approval from the U.S. Food and Drug Administration for a fast, easy-to-use test for novel coronavirus infections. At first glance, ...

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FRANKLIN LAKES, N.J., Dec. 22, 2021 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical company, today announced the BD Veritor™ At-Home COVID-19 Test is now ...

As the world continues to have a need for COVID-19 testing, BD offers a reliable rapid antigen COVID-19 testing solution through the BD Veritor™ System for Rapid Detection of SARS-CoV-2*. This ...

The newly launched BD Veritor At-Home COVID-19 Test uses AI technology to promote better accuracy by reducing human error and allows you to share your results ...

correctionA previous version of this article incorrectly said that Detect's Starter Kit contains two tests. It contains one. The article has been corrected. In January, the government promised each ...

Becton, Dickinson and Company BDX — also popularly known as BD — recently received CE mark for its rapid, point-of-care, SARS-CoV-2 antigen test for utilization on the BD Veritor Plus System. The new ...

NEW ORLEANS--(BUSINESS WIRE)--Ready, an on-demand healthcare service, today announces in-home rapid COVID-19 testing with results in 15 minutes or less. The rapid test can be run from start to finish ...

BD VERITOR SYSTEM FOR RAPID DETECTION OF FLU A + B by BD Diagnostics BD Diagnostics announced that it has received clearance from the FDA for nasopharyngeal wash, aspirate, and swab in transport media ...

New Jersey-based medical technology company Becton Dickinson, or BD, is conducting an investigation following reports that its COVID-19 point-of-care testing equipment is producing false positive ...

Becton, Dickinson and Company BDX, popularly known as BD, recently announced receipt of the FDA’s Emergency Use Authorization (“EUA”) for the BD Veritor At-Home COVID-19 Test. The test is an ...

Becton, Dickinson and Company BDX, popularly known as BD, recently announced receipt of the FDA’s Emergency Use Authorization (“EUA”) for the BD Veritor At-Home COVID-19 Test. The test is an ...