04:12 pm March 30, 2020
The weaknesses highlighted by the FDA in Urgent/11 demonstrate there are susceptibilities within software platforms that are both identifiable and resolvable.
04:51 pm August 16, 2019
Medical devices must be managed from a security perspective, but also from an operational perspective. Using analytics to establish behavior baselines helps support risk assessments, find malfunctions and enhance staff productivity.
03:49 pm June 16, 2017
Feeding data directly from a medical device into medical records has reduced errors, improved patient safety and increased caregiver efficiency.
06:43 pm January 09, 2017
Most medical things exhibited at CES 2017 are connected devices with apps that collect, analyze, and feedback data and information to users (patients, consumers, caregivers) and health/care providers (physicians, nurses, care coaches, and others who support people in self-care).
07:23 am August 08, 2016
Penn Medicine associate vice president of health technology Brian Wells shares insights from cognitive computing work so far.
01:48 pm May 05, 2016
At the start of 2016, the current installed base of wearable activity tracking devices was just over 33 million in the U.S.
10:51 am March 25, 2016
"We believe that mobile devices such as iPhones will become the predominant means by which patients interact with BIDMC," says Beth Israel Deaconess Medical Center CIO John Halamka, MD. "Your phone will be the repository of your medical record."
06:41 am November 02, 2015
(SPONSORED) As timing and accuracy of data are key components to the efficiency, speed, and therefore overall costs of operating a clinical trial, consumer wearables offer an unparalleled opportunity to remedy these issues.
10:57 am October 12, 2015
(SPONSORED) If the prospect of hackers honing in on medical devices makes you uneasy, it should. Medical devices are being exploited as entry points for deeper attacks on systems within a healthcare organization.
06:09 am September 09, 2015
Broadly defined, software as a medical device is any app used by providers to make clinical decisions. An increasing number of those are now officially designated as FDA-regulated devices. Is it worth it to pursue this classification for your own software?