Patient Care

This page includes news coverage of various aspects of patient healthcare, including new technology innovations, what is working, what is not, personalized medicine and remote and telemedicine delivery. Find specific news in the areas of Care DeliveryDigital TransformationPrecision MedicineRemote Monitoring and Telehealth.

NIBIB sponsors student challenge to create new technologies

The National Institute of Biomedical Imaging and Bioengineering (NIBIB), part of the National Institute of Health, will host a competition for undergraduate students to design and develop new diagnostic and therapeutic devices, as well as new technologies to help underserved communities and the disabled.

RSNA: Radcal, VacuTec partner for dose area product meter release

Radcal (booth 3705) is partnering with Dresden, Germany-based VacuTec to release the Dose Area Product (DAP) meters, VacuDAP, in North America. The Monrovia, Calif.-based manufacturer is displaying the product at the 97th Annual Meeting & Scientific Assembly of the RSNA, Nov. 27 to Dec. 2, in Chicago.

Mercy to open $680M virtual care center

Mercy, a health system covering four Midwestern states, is planning to open a virtual care center near its headquarters in Chesterfield, Mo.

Landauer buys IZI Medical for $93M

Glenwood, Ill.-based medical physics services provider Landauer has acquired Baltimore-based IZI Medical Products for $93 million. IZI sells products related to radiology, radiation therapy and image guided surgery procedures, and was previously owned by Boston-based Riverside Partners.

Consumers Union calls for improved medical device safety

In a Nov. 15 letter to members of Congress, Consumers Union urged reauthorization of the Medical Device User Fee Actcurrently set to expire Sept. 30, 2012and outlined ways to improve oversight of medical device clearance processes. The letter appeared Tuesday morning prior to a meeting of the Senate Health, Education, Labor and Pensions Committee on medical devices.

FDA's Shuren testifies in favor of reauthorizing device user fee

Responding to industry-wide scrutiny of the clearance process for medical devices, Jeffrey Shuren, MD, director of the FDA's Center for Devices and Radiological Health (CDRH), said a root cause of the perceived lack of predictability, consistency and transparency is funding.

Positron makes purchase to enter radioisotope business

Molecular imaging company Positron has signed a letter of intent to buy Manhattan Isotope Technology (MIT), a strontium-82 (SR-82) product specialist, for an undisclosed amount.

Image Gently, SNM launch pediatric dose reduction campaign

The Image Gently campaign and the Society of Nuclear Medicine (SNM) have launched the Go With the Guidelines campaign to encourage community hospitals, academic hospitals and clinics to observe new North American Guidelines for Nuclear Medicine Radiopharmaceutical Dose in children.

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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