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Home » SARS-CoV-2

Articles Tagged with ''SARS-CoV-2''

Regulatory actions for March 20, 2020

March 20, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Genmark Dx.
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Other news to note for March 20, 2020

March 20, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aino Health, Alector, Biodesix, Bio-Rad Laboratories, Boqi International Medical, Carecentrix, Caredx, Cerveau Technologies, Chongqing Guanzan Technology, Co-Diagnostics, Danaher, Daxor, Firetinas, Lucence, Masimo, Mike Curtis Reward Solutions, Milliken, Mutual Mobile, Novocure, Precision Biomonitoring, RTI Surgical, Sartorius Stedim Biotech, Shandong Forward Medical Group, Soliton, Topcon Healthcare Solutions, Vitaltech.
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In the clinic for March 20, 2020

March 20, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Bio-Rad Laboratories.
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3-20-SCANWELL-COVID-19-App.png

Scanwell Health aims to broaden COVID-19 testing with at-home tests

March 20, 2020
By Meg Bryant
With the number of COVID-19 cases continuing to rise and with people social distancing and quarantining, at-home diagnostics and telehealth offer the means for doctors and patients to get vital answers and care without meeting face to face. Now, Los Angeles-based Scanwell Health has gained exclusive rights to license and distribute a rapid serology test from Innovita Biological Technology Co. Ltd., of Hebei, China, for at-home testing of SARS-CoV-2, the coronavirus that causes COVID-19.
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Other news to note for March 19, 2020

March 19, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alibaba Cloud, Avellino Labs USA, Aytu Bioscience, Bio-Rad Laboratories, Boqi International Medical, Chongqing Guanzan Technology, Co-Diagnostics, Cosara Diagnostics, Endra Life Sciences, Medtronic, Milken Institute, Novocure, Paragon Genomics, Vitalhub, Vizient, Zorion.
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Regulatory actions for March 19, 2020

March 19, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbott, CHF Solutions, Qiagen.
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Regulatory front for March 19, 2020

March 19, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: CME America, Mesa Biotech.
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Coronavirus and DNA

FDA greenlights emergency use of Abbott SARS-CoV-2 test

March 19, 2020
By Meg Bryant
Abbott Laboratories, of Abbott Park, Ill., is the latest company to receive emergency use authorization (EUA) from the U.S. FDA for a test to detect SARS-CoV-2, the novel coronavirus responsible for the COVID-19 pandemic. The company said it is shipping 150,000 Realtime SARS-CoV-2 tests immediately to existing customers in the U.S., with plans to produce 1 million tests a week by the end of the month.
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U.S. flag and White House podium

Defense Production Act invoked as larger volume of ventilators identified

March 19, 2020
By Mark McCarty
President Donald Trump has issued an executive order enabling the Defense Production Act, which gives the U.S. Department of Health and Human Services broader leeway to conscript industrial production to deal with the COVID-19 outbreak.
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Actemra product packaging

Genentech moves Actemra into phase III COVID-19 trial

March 19, 2020
By Cormac Sheridan
DUBLIN – The Genentech arm of Basel, Switzerland-based Roche Holding AG plans to move its interleukin-6 (IL-6) inhibitor, Actemra (tocilizumab), into a global phase III trial in patients with severe pneumonia associated with COVID-19 infection.
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