Organization

European Union


GE releases tiny, point-of-care ultrasound

New Products | Monday, February 15 2010
 

Study: Implementing EHR, e-prescribing is challenging, but beneficial over time

Top Stories | Sunday, January 10 2010
 

Merge, Medrad agree to expand CAD product distribution in EU

Partnerships & Alliances | Friday, October 30 2009
 

EDAP nets FDA approval for ultrasound device

Regulatory News | Thursday, August 20 2009
 

FDA, EMEA launch initiative to better clinical trials

Industry News | Tuesday, August 04 2009
 

Pressure to curb MRI restrictions in EU builds

Industry News | Friday, May 22 2009
 

Japan to speed arduous medical device approvals with new plan

Industry News | Tuesday, January 06 2009
 

Siemens PETNET poised to up NaF production during shortage

Industry News | Tuesday, October 07 2008
 

Germany to begin distributing electronic health cards

Industry News | Wednesday, December 31 2003
 

FDA further approves Stereotaxis' magnetic irrigated catheter

Regulatory News | Thursday, January 14 2010
 

EU greenlights VentriPoint's heart disease monitor

Regulatory News | Friday, December 11 2009
 

Philips' project develops hybrid PET/MR

New Products | Thursday, October 29 2009
 

EU survey: Public overestimates benefits of cancer screening

Clinical Studies | Tuesday, August 11 2009
 

Covidien completes HQ move to Ireland

Industry News | Tuesday, June 09 2009
 

Covidien moves headquarters to Ireland

Industry News | Tuesday, January 06 2009
 

EU creates Ebay for radiologists

Industry News | Wednesday, October 15 2008
 

EMEA addresses radioisotope shortage; appeals to private industry

Top Stories | Thursday, October 02 2008
 


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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