Organization

Robert Wood Johnson Foundation


New rankings provide county-to-county health snapshots

Industry News | Friday, February 19 2010
 

Survey: Nurses should have stronger voice in healthcare decision making

Industry News | Tuesday, January 26 2010
 

Report: Health IT central to healthcare debate

Industry News | Wednesday, October 28 2009
 

Survey: 75% of physicians accepting new Medicare patients

Top Stories | Friday, September 04 2009
 

Physician practice, payor interactions cost $31B annually

Top Stories | Friday, May 15 2009
 

NEJM: Less than 2% of hospitals have comprehensive EHR—stimulus might help

Top Stories | Wednesday, March 25 2009
 

U.K. $19B EMR project plagued with setbacks

Top Stories | Wednesday, October 29 2008
 

Report: Physicians' efforts to reduce racial, ethnic inequalities modest

Industry News | Thursday, February 11 2010
 

Study: EHR adoption encouraged for providers serving the poor

Clinical Studies | Wednesday, October 28 2009
 

NEJM: Most AMA docs support expanding healthcare coverage—with choice

Industry News | Tuesday, September 15 2009
 

Patients willing to forgo some health IT privacy for availability

Clinical Studies | Wednesday, May 20 2009
 

Robert Wood Johnson Foundation calls for health IT grant proposals

Industry News | Tuesday, April 14 2009
 

HIPAA privacy rule fails to protect patients, hampers health research

Top Stories | Thursday, February 05 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