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.
Healthcare is becoming a significant force in addressing environmental challenges, with hospitals reporting clear progress on sustainability. Fresh benchmark data points to measurable environmental gains across healthcare, alongside stronger governance and clearer targets.
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Health technology leaders have shared their insights in response to a letter published by NHS England’s Chief Executive Jim Mackey.
The letter outlines strategies to improve waiting times, enhance community care, and use digital solutions for sustainable healthcare transformation.…