The influx of patient data has opened the doors to innovation in patient care. Discover how to use data and analytics to enable value-added innovation in this webinar.
The independent data safety monitoring board found the clinical trial needs to keep enrolling patients and gather results to show if the treatment works.
The healthcare giant was the first procedure-dependent medtech to announce earnings this quarter, potentially foreshadowing what others in the industry will report in the coming weeks.
FDA said use of the tests before the problem is corrected may cause serious adverse health consequences or death, alerting laboratories to treat the results as presumptive and that they may need to be confirmed with another test.
On average, U.S. hospitals have from 10 to 15 connected devices per bed. Learn how medtechs are prioritizing security throughout the product development process to decrease breach risks post-market in this playbook.
Megan Rosengarten spoke to MedTech Dive about challenging Intuitive Surgical's 20-year lead in soft tissue robotics, growing global robotics usage and the stress of entering a new market amid COVID-19.
William Blair analysts warn that limited provider support during the medtech's recall is hurting brand credibility and impacting Philips' ability to regain market share, while positioning ResMed as the beneficiary of "durable" share loss.
"It truly is like we are operating in about the 1950s," one consultant noted of the process. The FDA has held two meetings in the past year to mull improvements.
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