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Intellectt, Inc. Acquires U.S. Electronics, Inc. to Bolster Medical Device Manufacturing and Staffing Expertise

Imaging Technology

(USEI), a reputable medical device manufacturing company with over 25 years of experience announced it has been acquired by Intellectt, Inc., as it expands its capabilities in the healthcare industry with its 7th acquisition in the Life Science/Healthcare sectors within the prior two years. Intellectt, Inc.

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Why Enterprise-Wide AI Requires Image- and Report-Based AI

Aidoc

Furthermore, is there a way to combine the powers of different types of AI, such as image and report based AI, to create better care opportunities? From day one, Aidoc has understood that image-based AI is crucial to prioritize urgent cases and augment radiologists, thus improving quality of care.

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AI in Healthcare: The Ultimate Guide

Aidoc

Over 700 devices are categorized as “artificial intelligence and machine learning enabled medical devices” on the FDA website. This may create the perception that all AI in healthcare is the same. Imagine healthcare as a large system with many moving parts. What is AI?

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3 Service Strategies for Medical Imaging Equipment in 2023

Everything Rad

As we enter 2023, we see familiar – and essential – service strategies for maximizing the return on investment (ROI) on medical imaging equipment: Strengthen cybersecurity to keep operations flowing. 1) Medical imaging software that is not in synch with vendor upgrades can be vulnerable to hackers.

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Extend the Life of Your X-ray Imaging Equipment

Everything Rad

How would you rate the value you are getting from your current X-ray imaging equipment? Does it support new medical imaging software that can help improve clinical outcomes? Upgrade your X-ray imaging equipment to get access to the most advanced imaging features for about 10% of the cost of original equipment.

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AI in Radiology: Biden’s New Executive Order and Latest News

Vesta Teleradiology

The order aims to ensure responsible use of AI in healthcare and establish a federal program to address unsafe practices. The FDA premarket review for medical devices like CAD programs is likely to be augmented with additional quality and equity requirements.