Organization

Advanced Medical Isotope Corporation


USPSTF recommends cutting annual breast screening

Top Stories | Tuesday, November 17 2009
 

AMIC: MedPAC proposed 90% equipment utilization rate is unrealistic

Industry News | Thursday, September 10 2009
 

ACR lobbies to change aspects of healthcare reform

Industry News | Monday, August 17 2009
 

House healthcare reform bill calls for 75% increase in imaging utilization

Top Stories | Wednesday, June 24 2009
 

AMIC launches imaging Web site

Industry News | Monday, May 18 2009
 

AMIC counters MedPAC imaging report

Top Stories | Monday, March 16 2009
 

Report: Imaging utilization has decreased since DRA

Industry News | Tuesday, October 20 2009
 

Survey: Medical imaging should not be subject to Medicare cuts in reform

Industry News | Wednesday, September 09 2009
 

AMIC questions CMS utilization rate increase

Industry News | Friday, July 10 2009
 

RBMA: MedPAC imaging use rates far above reality

Top Stories | Friday, June 19 2009
 

AMIC responds to Senate proposals for new imaging policies

Top Stories | Friday, May 01 2009
 

AMIC: MedPAC medical imaging report flawed, should be rejected

Top Stories | Thursday, February 26 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.

PORTALS