Eli Lilly and Company's bebtelovimab receives Emergency Use Authorization for the treatment of mild-to-moderate COVID-19
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FDA has authorized bebtelovimab for emergency use for certain non-hospitalized patients with mild-to-moderate COVID-19 at high risk of progression to severe disease for whom alternative COVID-19 treatment options approved or authorized by FDA are not accessible or clinically appropriate Bebtelovimab neutralizes Omicron as demonstrated by pseudovirus and authentic virus data.
The rapid evolution of artificial intelligence (AI) offers transformative opportunities in healthcare. However, to fully realise this potential, it is important to build strong foundations in education and research.
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It is important the UK keeps control of NHS data in order to protect patients, Prime Minister Sir Keir Starmer has said, as he insisted it was also important companies can make use of it.
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