AuntMinnie
FEBRUARY 1, 2024
“Transparency is the degree to which appropriate information about a device – including its intended use, development, performance, and, when available, logic – is clearly communicated to stakeholders,” the group wrote. The full article is available here.
MRI Network
JANUARY 8, 2024
Healthcare is a fast-evolving landscape driven by transforming technologies and shifting user requirements. The need for more remotely accessible services like telemedicine and a range of advanced medical devices is accelerating growth across the industry. Medical Device Sales: Which Devices Are Driving Industry Growth?
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MRI Network
JUNE 2, 2024
Artificial intelligence has already had a tremendous influence on the healthcare industry. Today, professionals use AI and machine learning to process massive amounts of data quickly, find patterns that predict emerging health issues within communities, and diagnose patients more accurately, among other things.
MRI Network
MARCH 10, 2024
Post-pandemic, it’s clearer than ever that medical professionals and care facilities need innovative ways to communicate with patients and provide relevant care. This health-specific information is then sent over the internet to the doctor or other medical professional in charge of monitoring the patient’s data.
AuntMinnie
APRIL 19, 2023
has joined Nuance Communication'. Read more on AuntMinnie.com Related Reading: Nuance releases new AI healthcare documentation app Qure.ai secures EU medical device regulation certification Qure.ai Artificial intelligence (AI) software developer Qure.ai secures FDA clearance for qER-Quant
Imaging Technology
NOVEMBER 14, 2023
“We are thrilled to introduce our latest innovation in Women's Health and Urology imaging, reflecting our unwavering commitment to delivering efficient care and meeting the imaging demands of medical professionals,” said David Legg , Head of Boston Imaging.
Vesta Teleradiology
JULY 31, 2023
However, the FDA has not reviewed these devices, and they lack the necessary 510(k) clearance or premarket approval. FDA to evaluate and approve medical devices. The FDA reviews the submission to ensure the new device shares the same intended use and technology as the predicate device. What is 510(k) Clearance?
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