Difference between revisions of "Hoffmann-La Roche"

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(nCoV-2019 antibody test)
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==nCoV-2019 antibody test==
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Mai, 2020: The test is the third granted ''emergency approval by the [[FDA]]'' in a urgent procedure and the first commercially available. It gives quick results (18 Min.) and will be accepted worldwide in what has been touted one of Roche's biggest deals. <ref>
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https://www.marketwatch.com/story/roche-coronavirus-test-gets-emergency-fda-approval-2020-03-13
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The test is not based on the PCR method (which directly detects parts of viral RNA) but addresses antibodies built by the immune system after 1-2 weeks of contact. These may not be specific with a risk for false positives stemming from common cold viruses. The test is self-approved by Roche with the FDA merely giving green light. <ref>
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https://www.deutsche-apotheker-zeitung.de/news/artikel/2020/04/14/antikoerpertests-auf-corona-risiko-von-fehlinterpretation
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Revision as of 12:06, 6 May 2020

Main.png Hoffmann-La Roche  
(Big pharma)Rdf-entity.pngRdf-icon.png
Roche.svg
Formation1896
FounderFritz Hoffmann-La Roche
Member ofAlliance for Biosecurity, European Policy Centre
Founder ofDiazepam
SubpageHoffmann-La Roche/President

nCoV-2019 antibody test

Mai, 2020: The test is the third granted emergency approval by the FDA in a urgent procedure and the first commercially available. It gives quick results (18 Min.) and will be accepted worldwide in what has been touted one of Roche's biggest deals. [1] The test is not based on the PCR method (which directly detects parts of viral RNA) but addresses antibodies built by the immune system after 1-2 weeks of contact. These may not be specific with a risk for false positives stemming from common cold viruses. The test is self-approved by Roche with the FDA merely giving green light. [2]


 

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References


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