Organization

Office Of The Inspector General


OIG: Adverse event reporting process varies regionally

Industry News | Friday, January 15 2010
 

CMS, ARRA health IT programs slated for OIG audit

Top Stories | Tuesday, November 03 2009
 

Feature: Imaging payments, appropriateness under OIG review

Top Stories | Monday, October 12 2009
Written by Jeff Byers
 

OIG: Medicaid isn't properly detecting fraud

Top Stories | Tuesday, September 15 2009
 

OIG cautions CMS about ultrasound overuse

Top Stories | Sunday, July 26 2009
 

Report: Hospitals need more accountability, oversight of physician discipline

Top Stories | Monday, June 01 2009
 

Three cardiologists settle for $355K over Stark Law violations

Top Stories | Tuesday, March 24 2009
 

MedQuist pays $6.6M to DoJ for overbilling

Top Stories | Thursday, December 04 2008
 

Minnesota Hospital settles whistleblower suit

Top Stories | Thursday, January 07 2010
 

OIG asserts FDA's CDRH is not efficient

Industry News | Friday, October 30 2009
 

News & Views

Departments | Tuesday, September 22 2009
Written by Justine Cadet
 

OIG: VA's integration problems reflect system-wide IT issues

Industry News | Wednesday, September 09 2009
 

Task force uncovers $50M in alleged Medicare fraud; 53 arrested

Top Stories | Wednesday, June 24 2009
 

Radiologists to pay $2M in Medicare fraud settlement

Top Stories | Monday, March 30 2009
 

DoJ joins whistleblower suit against N.M. health system

Top Stories | Monday, March 09 2009
 

OIG slams CMS for lack of HIPAA compliance enforcement

Top Stories | Monday, November 03 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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