Person

Mark Leavitt


CCHIT: IFR underestimates regulatory economic impact

Industry News | Friday, March 12 2010
 

CCHIT to launch ARRA certification program next month

Industry News | Tuesday, September 08 2009
 

CCHIT proposes three EHR certification paths

Industry News | Friday, June 19 2009
 

CCHIT changes timelines

Industry News | Monday, June 01 2009
 

CCHIT develops task force; names 09 EHR pilot participants

Industry News | Thursday, April 16 2009
 

CCHIT expands, seeks comments on HIE certification

Industry News | Monday, February 23 2009
 

CCHIT: $20B IT investment would jump-start healthcare

Top Stories | Thursday, January 22 2009
 

CCHIT chair to retire in March 2010

Executive Announcements | Friday, November 13 2009
 

CCHIT seeks input on new EHR certification pathways

Industry News | Tuesday, August 25 2009
 

CCHIT seeks input on new EHR certifications

Industry News | Wednesday, June 10 2009
 

CCHIT changes program criteria to meet stimulus requirements

Industry News | Wednesday, May 20 2009
 

CCHIT ramps up certification efforts, extends volunteer deadline

Industry News | Wednesday, March 25 2009
 

Healthcare IT poised to gain ground

Editorial | Thursday, January 22 2009
 

CCHIT to expand certification programs

Industry News | Friday, January 16 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