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The President goes virtual

Thursday, March 04 2010
 

Should CMS reimburse for CTC?

Thursday, February 04 2010
 

Hybridizing Molecular Imaging

Tuesday, December 22 2009
 

Advanced technology: Its use and abuse

Thursday, December 10 2009
 

What Patients Want

Monday, November 09 2009
Written by Mary C. Tierney, Editorial Director
 

Integration delivers practice power

Thursday, October 22 2009
 

Advanced visualization: Cutting costs, dose

Thursday, October 08 2009
 

HITECH: Still musing on 'meaningful'

Thursday, September 17 2009
 

Advanced visualization offers new practice possibilities

Thursday, September 03 2009
 

Integrated, interoperable IT tools poised for takeoff

Thursday, August 20 2009
 

m-health in the developing world

Thursday, February 11 2010
 

Invasion of the Body Scanners

Thursday, January 07 2010
 

Integration and radiation

Friday, December 18 2009
 

Shuddering at Shuttering

Monday, November 09 2009
 

Now and future molecular imaging

Thursday, October 29 2009
 

PACS, DICOM and dose

Thursday, October 15 2009
 

Montreal makes it molecular

Thursday, September 24 2009
 

Liver cancer reports gain structure

Thursday, September 10 2009
 

Making molecular strides in Alzheimer’s diagnosis

Thursday, August 27 2009
 

RIS/PACS: Doing more, faster

Thursday, August 13 2009
 


Web Exclusives

AHRQ: Health IT could be disruptive while reducing rehospitalization rates, costs

 The use of health IT to reduce rehospitalizations will be welcome but also disruptive, said Stephen Jencks, an independent consultant in healthcare safety during a Feb. 24 webinar on the potential use of health IT to mitigate rehospitalizations, sponsored by the Agency for Healthcare Research and Quality (AHRQ).

Health IT Standards Committee: Clinical Operations group seeks specificity in standards

 During the Health IT Standards Committee meeting on Feb. 24 in Washington, D.C., the Clinical Operations Workgroup sought to gather comments on proposed recommendations on implementation specifications for content exchange, vocabulary and code set standards for the Interim Final Rule of meaningful use.

Webinar: How-to guide for e-medical device reporting to the FDA

 In 2006, the Center for Devices and Radiological Health (CDRH), a branch of the FDA, began examining the number of medical device reports they received. Over the past two years, the number of submitted reports has increased, sparking a demand for the CDRH to make a move to electronic reporting.

New patient monitoring model draws scrutiny

 A new hospital breaking ground usually isn’t breaking news. But the vision of patient care at one new facility, tentatively named Palomar Medical Center West (PMC West), is currently illegal under California state law.

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