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Regulatory Compliance and Approval Processes in Medical Devices

Open Medscience

Medical Device Regulatory Compliance ensures safety and effectiveness through stringent testing and approval processes globally. The post Regulatory Compliance and Approval Processes in Medical Devices appeared first on Open MedScience.

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GE HealthCare to Spotlight Industry-Leading AI-Enabled Portfolio and Digital Solutions at HIMSS 2024

Imaging Technology

milla1cf Thu, 03/07/2024 - 20:10 March 7, 2024 — GE HealthCare will showcase its industry-leading portfolio of artificial intelligence ( AI )-enabled medical devices and digital solutions in Booth 2500 at the Health Information and Management Systems Society ( HIMSS ) Global Health Conference and Exhibition in Orlando, FL from March 11-15, 2024.

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MedDream Integrates Viewer with AWS HealthImaging

Imaging Technology

Because of this integration, in case of a PACS disruption, physicians can access studies directly through the MedDream DICOM Viewer, thus allowing for uninterrupted diagnostics, patient care and operational efficiency. “We We are excited about working with AWS to leverage AWS HealthImaging,” says Tomas Dumbliauskas, MedDream CEO.

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Not All AI Is Equal: A Comparative Study of Three Imaging Algorithms

Aidoc

The adoption of artificial intelligence (AI) in medical imaging has experienced substantial growth in recent years, with more than 450 AI-based medical devices gaining approval in both Europe and the USA. Vendor B 62.8%

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How can Enterprise Imaging empower radiology in the modern health network?

AuntMinnie

Worklists optimize the display of studies from multiple institutions and systems, including third-party PACS. “We Mayer is a 30-year-plus veteran in the healthcare information technology (HIT), EI, and the medical device field. We want to share and collaborate."

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Ensuring Compliance: Industrial Challenges in Meeting EU MDR

Open Medscience

Ensuring compliance with EU MDR poses significant challenges for medical device manufacturers, including increased scrutiny, financial strain, and data protection demands. The post Ensuring Compliance: Industrial Challenges in Meeting EU MDR appeared first on Open MedScience.

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New Version of aycan Workstation Supports Big Data

Imaging Technology

is certified under the new European MDR (Medical Device Regulation). aycan workstation is an FDA 510(k) cleared, vendor-neutral, highly functional advanced image-processing tool and DICOM PACS workstation for conventional, multi-slice, and other image reading with clinical and workflow plugins that further enhance its capabilities.

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