FDA approval for Yescarta in follicular lymphoma makes it the first approved CAR-T treatment for this type of cancer. It also marks Gilead Sciences’ third approved indication for a CAR-T…
Abbott announced the launch of the newly-approved NeuroSphere Virtual Clinic by which deep brain stimulation patients can have their devices programmed and reset remotely, from the comfort of their homes…
As the Department of Health and Human Services purchases more of Abbott’s rapid antigen tests, competitor Beckman Coulter said it is seeking an emergency use authorization for its $4 antigen…
Opportunities are set to appear at the intersection of technology, consumerism, and markets for those willing to move past their traditional limitations. The healthcare industry is rapidly shifting toward more…
The authorization comes as Covid-19 testing demand threatens to swamp U.S. labs. However, it will take time for the Lucira test to become available nationwide. Read more
Placing orders for the wrong patient, though rare, can lead to serious harm if left unchecked. Brigham and Women’s Hospital implemented a simple protocol that lowered these errors by 35%.…
CMS’ interim rule states that Medicare will cover Covid-19 vaccines approved by the FDA, including those receiving emergency use authorization, in a reversal from its usual policy. The vaccine will…
The disruption to biopharma and medtech businesses caused by Covid-19, from sales rep visits with doctors, product launch and clinical trial delays has underscored the need for a more digital…
The FDA granted an emergency use authorization to an algorithm developed by Dascena to predict which Covid-19 patients might face unstable blood pressure or respiratory decline. Read more
Long before the start of the Covid-19 pandemic, the U.S. Department of Defense and Royal Philips had been working on a project to detect potential outbreaks of infectious disease before…
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