Difference between revisions of "Hoffmann-La Roche"

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(nCoV-2019 antibody test)
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#REDIRECT[[Roche]]
|wikipedia=https://en.wikipedia.org/wiki/Hoffmann-La_Roche
 
|constitutes=Big pharma
 
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|logo=Roche.svg
 
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|start=1896
 
|founders=Fritz Hoffmann-La Roche
 
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==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. <ref>
 
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>
 
https://www.deutsche-apotheker-zeitung.de/news/artikel/2020/04/14/antikoerpertests-auf-corona-risiko-von-fehlinterpretation
 
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==References==
 
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Latest revision as of 22:33, 1 March 2022

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