Siemens Healthcare has announced that the Food and Drug Administration (FDA) has cleared the Magnetom Prisma, a 3 Tesla (3T) magnetic resonance imaging (MRI) scanner capable of extraordinarily high spatial and temporal resolution to achieve outstanding image quality, particularly in highly demanding applications.
Following public comment received in the fall of 2013, The Joint Commission has released new accreditation standards for diagnostic imaging services. Nearly all of these new standard Elements of Performance (EP) are slated to become effective in a half-year.
As breast density becomes a more recognized risk factor for breast cancer, Royal Philips announced 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Spectral Breast Density Measurement Application for its MicroDose SI full-field digital mammography (FFDM) system. The application is the first spectral Breast Density Measurement tool, meaning adipose (fat) and glandular tissue can be differentiated to accurately measure volumetric breast density.
eHealth Saskatchewan plays a vital role in providing IT services to patients, health care providers, and partners such ...
Piramal Imaging announced today the European Union's Committee for Medicinal Products for Human Use (CHMP) recommended approval of NeuraCeq (florbetaben 18F). The CHMP's recommendation will now be referred to the European Commission, for approval in the European Union (EU).
ViewRay Inc., a privately held medical device company, secured $30 million of funds to support the worldwide commercialization of the ViewRay system.

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Fujifilm Medical Systems U.S.A. showcased Aspire Bellus, a dedicated breast imaging workstation at the Radiological Society of North America Annual Meeting (RSNA 2013) in Chicago.
While most women understand the importance of health screenings, an estimated 72 million have missed or postponed a ...
Toshiba America Medical Systems Inc. introduced enhancements to its Vantage Titan magnetic resonance (MR) product line.
Mobius Medical Systems LP announced the release of the latest version of its flagship software product Mobius3D.
GE Healthcare showcased its SensorySuite “cocoon” experience at RSNA 2013. This 3-D fully-immersive video simulates SensorySuite by plunging participants into the overall SensorySuite patient experience. SensorySuite surrounds a woman with an interactive mammography experience designed to simultaneously stimulate three senses; sight, smell and hearing, helping to distract the patient from the perceived discomfort, pain and anxiety of a mammogram.
Fujifilm’s APERTO Lucent is a 0.4T mid-field, open MRI system addressing today’s capability and image quality needs ...
For the first time, researchers have confirmed an association between a common magnetic resonance imaging (MRI) contrast agent and abnormalities on brain MRI, according to a new study published online in the journal Radiology. The new study raises the possibility that a toxic component of the contrast agent may remain in the body long after administration.
The American College of Radiology (ACR) commends the House Committee on Ways and Means and the United States Senate Committee on Finance for passing bicameral, bipartisan legislation to replace the flawed sustainable growth rate (SGR) physician payment formula.
A new study by researchers at the University of California, Los Angeles (UCLA) Fielding School of Public Health and McGill University in Montréal reveals that the United States health care system ranks 22nd out of 27 high-income nations when analyzed for its efficiency of turning dollars spent into extending lives.
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Researchers have identified a potential biomarker for predicting whether a premature infant is at high risk for motor development problems, according to a study published online in the journal Radiology.
Ultrasound will be able to depict blood flow with more detail and accuracy using Toshiba America Medical Systems Inc.’s work-in-progress ultrasound capability, which is the latest advancement to Toshiba’s Aplio 500 ultrasound system.
By Dave Fornell, DAIC editor While the Radiological Society of North America (RSNA) focuses on new technology for radiology, it is where vendors formally introduce all their imaging systems, including those for cardiology. The annual RSNA meeting is also a barometer for new trends in imaging and imaging related information technology.
Double Black Imaging demonstrated its full line of auto-calibrating LED displays at the Radiological Society of North America Annual Meeting (RSNA 2013).
GE Healthcare announced its exclusive clinical application for its fixed radiographic system, VolumeRAD, at the Radiological Society of North America Annual Meeting (RSNA 2013).
Fujifilm Corp. introduced its latest digital mammography system, the Amulet Innovality, at the Radiological Society of North America Annual Meeting (RSNA 2013).
Most women who undergo partial mastectomy (lumpectomy) surgery for breast cancer also complete a course of radiotherapy delivered to the whole of the affected breast (called external beam radiotherapy, EBRT). EBRT has been shown to reduce the risk of cancer recurring in the breast, but it can cause unpleasant side-effects, and requires women to attend radiotherapy centres for 20 days after surgery, which can cause serious difficulties for women who live far from radiotherapy centres, especially those in remote or very rural areas. In some cases, women who are eligible for lumpectomy may end up undergoing full mastectomy, simply because they cannot meet the demands of subsequent radiotherapy treatment required by partial tissue removal.
Fujifilm Medical Systems U.S.A., Inc. highlighted its new floor-mounted digital X-ray system at the Radiological Society of North America Annual Meeting (RSNA 2013) in Chicago.