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28 February 2021 COVID19 EMERGENCY REGULATIONS ALERT LEVEL 3 These regulations apply to regions that are subject to Alert Level 3. If the government declares that there are domestic border restrictions,
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FDA announces Evusheld as a new monoclonal antibody therapy for COVID-19.
Healthcare providers and facilities are required to file for FDA approval to administer Evusheld.
The application to administer Evusheld must be filled out online on the FDA's website.
The purpose of FDA announcing Evusheld is to provide a new treatment option for COVID-19 patients.
The report must include details on the patient's demographics, medical history, and the administration of Evusheld.
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