Company

Bracco Diagnostics


FDA finds Bracco’s imaging agent is misbranded

Industry News | Tuesday, January 26 2010
 

MR technique delivers superior pelvic visualization

Portal Exclusives | Thursday, November 05 2009
 

AHJ: No difference between GE’s Vispaque and Bracco's IsoVue for adverse events

Clinical Studies | Wednesday, October 28 2009
 

Ultrasound growth driven by hand-carried devices

Industry News | Saturday, August 01 2009
 

Bracco wins $11.4M from GE for false advertising claims

Top Stories | Monday, March 30 2009
 

Bracco Diagnostics

Previews | Wednesday, October 29 2008
 

Bracco teams with Datalliance for vendor managed inventory program

Partnerships & Alliances | Thursday, January 21 2010
 

RSNA: Bracco/Acist Medical updates EmpowerCTA contrast injector

Conference News | Wednesday, October 28 2009
 

Reformations deliver diagnostic CT data

Portal Exclusives | Thursday, September 03 2009
 

JACC: Risk of kidney injury equivalent between iso- and low-osmolar contrast media

Clinical Studies | Wednesday, July 29 2009
 

Bracco showcases expanded portfolio

In Review | Tuesday, December 23 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.

PORTALS