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UDI, We’ve Only Just Begun
Healthcare Purchasing News
October 2014
The first official deadline associated with the Food and Drug Administration’s (FDA’s) Unique Device Identification (UDI) Rule has come and gone, but for manufacturers, their work around compliance has only just begun, explains Karen Conway, Industry Relations Director, GHX.

 

   

 

Perspectives - Ready for UDI
Medical Design Technology
October 2014
"Trust, but verify" is my advice for manufacturers seeking to comply with the UDI rule, says Steve Cochran, Chief Technology Officer, GHX.

 

   

 

GHX Successfully Submits Product Data to the FDA GUDID ahead of Deadline
Becker's Hospital Review
October 2014
One day before the U.S. Food and Drug Administration's (FDA) deadline for medical device companies to submit Class III product data to the FDA's Production Global UDI Database (GUDID), GHX announced that in August its UDI solution and services practice successfully submitted UDI data attributes in the required Health Level 7 Structured Product Label (HL7 SPL) format to the GUDID

 

   

 

5 Key Lessons to Successfully Prepare and Publish Data to the FDA’s GUDID
Medical Design Technology
October 2014
While the deadline for medical device companies to submit Class III product data to the FDA's Production Global UDI Database (GUDID) passed on September 24, 2014, the remainder of all medical device implantables, as well as products determined to be life-saving and life-sustaining, will now be subject to either the next deadline of September 2015 or the final deadline for Class II products of September 2016. Non-exempt Class I devices will follow, with a deadline of September 2018.

 

   

 

Top Five Skills Every Healthcare CEO Needs
Healthcare Business News
October 2014
Today's hospital CEO is faced with some of the most acute challenges to the health of provider organizations than at any time in the history of modern health care...

 

   

 

Are We Being Short-Sighted
Healthcare Purchasing News
September 2014
We’ve been talking about the benefits, as well as the costs, of the Food and Drug Administration’s (FDA’s) Unique Device Identification (UDI) Rule for years. Even now, as the rule is being implemented, the discussion, and debate, continues.

 

   

 

GUDID and GDSN - A Non-standard Deviation
Healthcare Purchasing News
September 2014
It’s D-Day, or I should say G-U-D-I-D Day, soon for manufacturers of class III medical devices that must be in compliance with the FDA’s Unique Device Identification (UDI) Rule as of September 24. Similar deadlines fall next year for all implantables and other life-saving and life-sustaining products regardless of class, in 2016 for Class II devices and in 2018 for non-exempt Class I products.

 

   

 

Let's Make the e-Procurement Vision an NHS Reality
Health Service Journal
August 2014
Ed Palferman at Global Healthcare Exchange (GHX) explains how the use of technology will be a step toward a successful NHS procurement system.

 

   

 

GHX Secures $5B in Supply Savings over Past 5 Years
Becker’s Hospital Review
August 2014
Louisville, Colo.-based GHX, a healthcare supply chain technology company, reports saving $5 billion in supply chain savings for the North American healthcare market over the past five years.

 

   

 

GHX Surpasses $5 Billion in Healthcare Savings
Healthcare Matters
August 2014
GHX and its supplier and provider customers have successfully accomplished the goal they set nearly five years ago – to secure $5 billion in supply chain savings for the North American healthcare market. This milestone marks the achievement of the company’s “5-in-5”goal, a commitment made in January 2010 to take $5 billion out of the cost of healthcare. - See more at: http://hcmatters.com/2014/08/ghx-surpasses-5-billion-healthcare-savings/#sthash.MYummR2D.dpuf

 

   

 

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