(Reuters) – Abbott Laboratories said on Friday that the U.S. Food and Drug Administration granted emergency use authorization for its molecular test to detect and
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Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. Tests to detect antibodies to SARS-CoV-2 are most sensitive among people
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Travel testing: Shapps reveals ‘concerns’ over South African variant Households in the Goldsworth Park and St John areas of Woking will asked to carry out
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