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CDC To Yank EUA On Original COVID-19 Test At Year’s End

 
• By Elizabeth Orr

The US body says it wants to encourage labs to use newer, faster alternatives that can also detect other pathogens.

UNINCORPORATED DEKALB COUNTY, GA -Â?Â? MARCH 30: The US Centers for Disease Control and Prevention headquarters on March 30, 2013. The CDC is the national public health institute of the United States.

The first COVID-19 test to be authorized by the US Food and Drug Administration will come off the shelves at the end of the year, the Centers for Disease Control and Prevention (CDC) announced on 21 July.

The CDC plans to withdraw its FDA request for an emergency use authorization (EUA) for the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR diagnostic panel as of 31 December to make...

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• By Brian Bossetta

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Commission’s Flora Giorgio Says Simplification And Safety Are Key In Evolving EU Regs

 
• By Amanda Maxwell

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More from Policy & Regulation

Swiss Medtechs Advised To Work On US Tariff Mitigation Strategies

 
• By Ashley Yeo

The US’ 90-day suspension of higher “reciprocal tariffs” will expire on 9 July, raising fears that the 31% tariff rate on Swiss medtech and other goods exported to the US might make a comeback. While the tariff situation changes on an almost daily basis, medtechs should forearm for any eventually, say local business organizations.

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• By Elizabeth Orr

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• By Vibha Sharma

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