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BD Taps Contract Packager for COVID-19 Test Kits

Photo supplied by Web Industries An operator at Web Industries in Massachusetts loads cassette magazines of test devices onto a Campbell Revolution Flow Wrapper. Using a form-fill-seal approach, the equipment packs each test kit, together with a desiccant pack, in a metallized pouch. With help from a nimble partner, medical device giant BD took its rapid COVID-19 test kit from concept to large-scale production in a matter of months. For many in medical packaging, 2020 was a year of pandemic pivots that forced changes to packaging lines and tested the agility of medical device makers, packagers, and equipment vendors alike. A successful case from the contract packaging space features BD (Becton, Dickinson and Co.) and its Veritor System for Rapid Detection of SARS-CoV-2 virus, which is an antigen test kit for COVID-19. BD announced in July 2020 that the US Food and Drug Administration (FDA) had granted Emergency Use Authorization (EUA) for the test kit.

USATF Partners With BD To Provide Rapid COVID-19 Testing To Enhance Athlete Safety At Track & Field Events

Share this article Share this article FRANKLIN LAKES, N.J., April 23, 2021 /PRNewswire/ USA Track & Field (USATF) and BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, have partnered to provide rapid COVID-19 testing for USATF athletes at Journey to Gold meets to help get USATF professional athletes back to competition safely through the use of the BD Veritor™ Plus system. USA Track & Field (USATF) and BD have partnered to provide rapid COVID-19 testing for USATF athletes at Journey to Gold meets to help get USATF professional athletes back to competition safely through the use of the BD Veritor™ Plus system.

FDA authorizes several OTC COVID-19 tests for routine screening

FDA authorizes several OTC COVID-19 tests for routine screening
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BD Receives Emergency Use Authorization for Asymptomatic Screening for SARS-CoV-2 through Serial Rapid Antigen Testing

Share this article Share this article FRANKLIN LAKES, N.J., April 1, 2021 /PRNewswire/  BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today announced the U.S. Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) for its rapid antigen test to be used for SARS-CoV-2 screening through serial testing of asymptomatic individuals. BD today announced the FDA has granted Emergency Use Authorization (EUA) for its BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 to be used for SARS-CoV-2 screening through serial testing of asymptomatic individuals. An elementary school student is receives a rapid antigen test using the BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2.

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