Kroger to Offer COVID-19 Rapid Antigen Home Tests
Kroger has plans to offer a new phone-enabled rapid test soon.
Kroger Health has partnered with Gauss and plans to offer the first smartphone-enabled, at-home COVID-19 Rapid Antigen Test Kit to people nationwide. The new test is currently awaiting Food and Drug Administration Emergency Use Authorization. After it is authorized, the rapid test can be fully performed using a smartphone and a nasal swab.
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Gauss has already produced the first 1.5 million tests that will be available for immediate distribution upon the Emergency Use Authorization from the FDA. When available, those tests will be up for purchase at kroger.com and at all 2,200 Kroger pharmacies nationwide. Gauss also has the capability of producing up to 30 million tests per month.
Kroger to Offer COVID-19 Rapid Antigen Home Tests banana1015.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from banana1015.com Daily Mail and Mail on Sunday newspapers.
/PRNewswire/ Kroger Health, the health care division of The Kroger Co. (NYSE: KR), today announced plans to offer the first smartphone-enabled, at-home.
NEW YORK, N.Y. (PRWEB) January 13, 2021 Ro, the healthcare technology company, and Gauss, the healthcare AI company, today announced a partnership to offer
Gauss Partners with Truepill in Strategic Effort to Deliver At-Home COVID-19 Rapid Testing to Millions
Share Article MENLO PARK, Calif. (PRWEB) December 23, 2020 Gauss, a leading developer of computer vision-aided diagnostics for healthcare, today announced its partnership with Truepill™, the digital health platform powering consumer health experiences through its API-connected infrastructure, to help facilitate the delivery of at-home COVID-19 rapid tests to customers’ doorsteps.
The partnership supports Gauss’s efforts to scale manufacturing and operations in advance of commercialization of its smartphone-powered at-home COVID-19 rapid antigen test, which has been submitted to the Food and Drug Administration (FDA) for Emergency Use Authorization (EUA).