Digital Transformation

This evolution of healthcare involves using technology to improve diagnosis, treatments, monitor patients, enhance hospital operations and culture, and bolster consumer-focused care. This includes virtual reality tools, wearable devices, workflow software, health apps and other digital health tools.

Boston Scis restructuring includes about 1,300 layoffs

Boston Scientific's restructuring plan includes standardizing and automating processes; relocation of activities; rationalization of the company reporting structure; and leveraging vendors. Under the plan, which is set to begin in the third quarter, an estimated 1,200 to 1,400 positions globally will be eliminated.

AFC launches equipment cart

AFC Industries has introduced the LB Series medical equipment cart.

Trial puts coiling on the MAP(S) for aneurysm treatment

Performing coiling in patients who suffer from both ruptured and unruptured aneurysm is safe and effective and showed high rates of post-procedure survival, according to the results of the MAPS trial presented at this years Society of NeuroInterventional Surgery meeting July 27 in Colorado Springs, Colo.

ASTRO elects new officers

The American Society for Radiation Oncology (ASTRO) has announced the results of its recent election. These new officers will begin their terms at the societys 53rd annual meeting in Miami Beach, Fla., which will be held Oct. 2-6.

Portable device diagnoses blood in minutes

A Columbia University researcher has reportedly developed a virtual lab-on-a-chip, which is able to diagnose tiny samples of blood within minutes and can be used in remote locations, according to study findings published online July 31 in Nature Medicine.

IOM to FDA: Scrap 510(k), start fresh

The Institute of Medicine (IOM) recommended the FDA scrap its 35-year-old 510(k) medical device clearance process and start anew, according to the findings of an evaluation released July 29, which chided the process as flawed, based on its legislative foundation.

FDA: Environment, user issues among risks in home medical devices

Home use medical devices are intended for patients to use in any environment, however, for that very reason they pose a number of risks and challenges which should be addressed by users and regulators, according to information provided in an FDA webinar July 28.

FDA's draft guidance may change medical device 510(k) review

As part of a plan to enhance predictability, consistency and transparency of premarket review programs, the FDA released draft guidance clarifying when medical device changes warrant new premarket review.

Around the web

The American College of Cardiology has shared its perspective on new CMS payment policies, highlighting revenue concerns while providing key details for cardiologists and other cardiology professionals. 

As debate simmers over how best to regulate AI, experts continue to offer guidance on where to start, how to proceed and what to emphasize. A new resource models its recommendations on what its authors call the “SETO Loop.”

FDA Commissioner Robert Califf, MD, said the clinical community needs to combat health misinformation at a grassroots level. He warned that patients are immersed in a "sea of misinformation without a compass."

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