The FDA has cleared a mobile application that will connect with a next-generation multiple daily injection automated insulin ...
BioPharma Consulting Group today announced the launch of a new digital transformation advisory framework designed to ...
Abstract: With the increasing population, the surge in vehicle owners has made parking challenges a pressing issue. Navigating a crowded parking lot in urban centers, commercial areas, and public ...
Edwards has received Food and Drug Administration approval for its Sapien M3 mitral valve replacement system, the company said Tuesday. The device is intended for people with moderate to severe mitral ...
On Monday, the U.S. Food and Drug Administration (FDA) approved Abbott Laboratories’ (NYSE: ABT) Volt PFA System to treat patients battling atrial fibrillation (AFib). AFib is the most common type of ...
Despite the earlier movement by competitors in PFA, Abbott CEO Robert Ford told investors in October that the company is “right on time, and we’re complete with the full portfolio.” The company hopes ...
Dr. Céline Gounder, an internist, epidemiologist and infectious disease specialist, is a CBS News medical contributor as well as senior fellow and editor-at-large for public health at KFF Health News.
The U.S. Food and Drug Administration has granted 510(k) clearance to 3D Systems, allowing its VSP Orthopedics virtual surgical planning and patient-specific instrumentation platform to benefit a ...
BGB-B2033 is a bispecific antibody directed at GPC3 and 4-1BB; key targets in the most common liver cancer FDA Fast Track Designation reflects the potential of BGB-B2033 in an area of high unmet need ...
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