GE HealthCare has received 510(k) clearance from the US Food and Drug Administration (FDA) for View, the diagnostic viewer within its Genesis Radiology Workspace.
The new solution is designed as a fast, zero-footprint diagnostic viewer and aims to streamline workflows and increase precision in radiological practice.
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Evidence indicates radiologists spend up to 44% of their time on tasks unrelated to image interpretation such as interface navigation or waiting for images to load.
This impacts productivity and turnaround times. There is increasing demand among radiology professionals for technologies that reduce turnaround time and enhance efficiency.
GE HealthCare solutions for enterprise imaging CEO Scott Miller said: “View is designed to meet radiologists wherever they are—providing secure, high-performance access to diagnostic imaging through a truly cloud native experience.
“By removing traditional infrastructure barriers, we’re enabling faster collaboration, greater flexibility, and more streamlined workflows across care teams. View within the Genesis Workspace reflects our commitment to modernising radiology in ways that support clinicians and, ultimately, improve patient care.”
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By GlobalDataView offers 2D and 3D visualisation, along with AI-based tools, to assist in clinical decision-making. Radiologists can work from virtually anywhere with full access to diagnostic features.
Direct access is provided to a range of advanced visualisation applications for comprehensive analysis within a single workflow.
Genesis Radiology Workspace comprises View, Workflow Manager and Enterprise Archive.
Last month, GE HealthCare launched its next-generation of LOGIQ ultrasound systems, designed to enhance clinical imaging and expedite workflows.
These systems introduce advanced imaging technologies, AI-powered automation, and an expanded digital platform to streamline daily diagnostic practices.
