Nathan Eddy works as an independent filmmaker and journalist based in Berlin, specializing in architecture, business technology and healthcare IT. He is a graduate of Northwestern University’s Medill ...

The International Medical Device Regulators Forum (IMDRF) has released a draft technical document to create a harmonized set of best practices in mitigating risks associated with the use of artificial ...

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Researchers at RIT have developed a new computer chip design approach that allows electronic systems to automatically adapt to real-world conditions, improving how devices manage power in everyday use ...

AI-enabled medical devices promise improved medical care and support for health care professionals. However, the safety and performance of such systems not only depends on algorithms or technical ...

App Store product pages will now display whether an app is a regulated medical device, Apple said today. The designation will be shown in the ‌App Store‌ in the European Economic Area (EEA), United ...

An Omaha, Nebraska, firm has been recommended to lead the $36 million design of a 1,500-bed men’s prison for the 400-acre campus that includes the existing circa-1878 men’s lockup in Concord. At its ...

To continue reading this content, please enable JavaScript in your browser settings and refresh this page. Preview this article 1 min Buffalo's medical device ...

Millions of Americans depend on medical devices — pacemakers, infusion pumps and patient monitors — to stay alive. But some of that equipment is made in China, and it may be spying on us – or worse.

New to Cricut? Learn everything you need to get started with Cricut Design Space in this complete step-by-step tutorial. #CricutTutorial #CraftingTips #DIYProjects 'Perfect storm': Trump berated a ...

Quality control is often still a manual process, particularly in medical device manufacturing. Vision inspection technology can help automate inspection, but manufacturers still face challenges.

Ransomware attacks on the healthcare sector surged by 30 percent in 2025, frequently disrupting operational technology and medical devices. FDA Section 524B mandates that manufacturers provide a ...