TEPR: CCHIT Meeting Draws Ire from Vendors, Ideas from Leaders



Loading...

BALTIMORE -- A “town hall” meeting of the Certification Commission for Healthcare Information Technology (CCHIT) at the annual Towards the Electronic Patient Record (TEPR) conference here this week turned into a shouting match at times, as small health-IT vendors were not shy about voicing their displeasure with the new program to certify ambulatory electronic health records (EHRs).

Joe Byers, a vice president of Juno Beach, Fla.-based Document Storage Systems (DSS), vociferously argued that the certification program now in place will accelerate consolidation, leading to small companies like his being swallowed up by a handful of large vendors.

When reminded that the testing was voluntary, Byers complained that no one would buy a product without a CCHIT seal of approval. Indeed, commission member Robert Tennant, government affairs manager of the Medical Group Management Association (MGMA), said, “Our members will be looking for certification.”

Small vendors were particularly upset about Tennant’s statement that forthcoming exemptions to Medicare anti-kickback regulations and the Stark rules on physician self-referral to allow hospitals and healthcare systems to supply health-IT to affiliated doctors likely require EHRs to have CCHIT certification.

If the Stark exemption includes such a requirement, “That is, in effect, federal law,” said Bill Sivill, a health-IT consultant at the meeting. “You are the tail wagging the dog.”

Department of Health and Human Services (HHS) officials are not commenting on the content of the final rules, which are due out at any time. However, the American Health Information Community (AHIC) advisory board on May 16 recommended that HHS accept the certification process. CCHIT has a three-year, $2.7 million HHS contract to create and administer a certification program for commercial EHR products.

The commission published the new ambulatory EHR standards May 1 and took applications May 3-12 (see http://www.health-itworld.com/newsletters/2006/05/02/19877?page%3aint=-1). Commission chairman Mark Leavitt, M.D., said that his staff received more than two dozen applications during the 10-day window and that about 175 people applied to be testing jurors.

Certification testing for 2006 costs $28,000, regardless of the size of the vendor seeking approval. Of that, $23,200 goes to the actual testing process and $4,800 is the annual fee to maintain certification. Vendors may use a certification for up to three years as long as they pay the annual maintenance fee, though they may choose to re-test annually to get a current-year certification stamp.

The cost and the renewal process were key targets of vendor ire. Several vendors promised that they will raise their prices if they have to pay the $28,000 testing fee. They also worried about spending money for a full re-testing next year so as not to appear that their products were out of date with a 2006 sticker in 2007.

Leavitt tried to assuage concerns by saying that certification will help business. “If you don’t see an acceleration in the [EHR] market, then we’ve failed,” he said.

Leavitt said that feedback from the health-IT community is causing him to think about how the recertification process will work starting next year. The commission plans on revising its standards annually. Still to be determined is how much testing will be required for a 2006-certified vendor to meet updated criteria in 2007.

Leavitt added that fees could come down in subsequent years, but that depends on future funding for the commission.

Click here to login and leave a comment.  

0 Comments

Add Comment

Text Only 2000 character limit

Page 1 of 1

White Papers & Special Reports

oracle_clinical
eClinical Visions - Clinical Trial Management: Enabling Operational Efficiency
Sponsored by Oracle

Read how contributors from Genzyme, Duke Clinical Research Institute, Accenture, Oracle Health Sciences and others address some of the most pertinent challenges facing the biopharmaceutical industry including... Globalization of clinical trials driven by the need to reduce costs and recruit participants; greater outsourcing; escalating regulatory demands; increased trial complexity; and post-marketing studies. Download this paper to gain new insight into:

  • Recent progress made in addressing these challenges
  • Expert opinion on clinical trial management systems (CTMS) for improving trial efficiencies
  • How to cut trial costs and enhance the productivity of trial participants


oracle_RDC
Remote Data Capture – Acquisition and Analysis
Sponsored by Oracle

Today nearly half of all clinical trials are conducted electronically, and rising! Electronic Data Capture (EDC) technology provides industry-wide opportunities, along with challenges, that are being addressed. In this informative report industry experts and users from Pfizer, PPD, C3i and Oracle Health Sciences discuss the impact of EDC and its newest zero footprint; online iteration.  It can used anywhere, world-wide, where the Internet is available while placing greater onus on global trial support. The critical focus of this new technology is that it must support the work of the person at the heart of the clinical trial system– the investigator. Download this report to learn more about:

  • Trends and Issues in an Electronic Clinical Data Management World
  • The New Remote Data Capture Paradigm 
  • Improving and Monitoring Clinical Data Management in the eClinical Age
  • Optimizing and Supporting Remote Data Capture


oracle_video
Technology Video Report: A Day in the Life with Remote Data Capture (Next-Gen EDC)
Sponsored by Oracle
See why Oracle Remote Data Capture (RDC) Onsite is the next generation in electronic data capture with its user-friendly method to collect, clean, review, and verify clinical trial data. Providing unprecedented performance with real-time data capture, Oracle RDC Onsite simplifies source data verification. With a clear, consistent view of study data across all sites, the benefits include reduced monitoring time, decreased queries and discrepancies, and less time to database lock.



Life Science Webcasts & Podcasts

Predict or Perish! Shaping the Practices of Clinical Trials
Decisionview webinarSponsored by:  DecisionView

Predictive Analytics are a key differentiator in running your clinical trials successfully through 2010 and beyond. They will help you to optimize your patient enrollment, reduce your clinical operations costs and minimize your financial liability in the clinical supply chain. In this session, you will:
• Learn what predictive analytics are and what they are not
• Understand why you need predictive analytics to run your clinical trials, and
• Explore how predictive analytics will shape the future of clinical trials

Download Now. 

 



More Podcasts

Job Openings

The University of Washington Department of Genome Sciences is seeking a LINUX SYSTEMS ENGINEERING MANAGER to lead a team in a diverse scientific computing environment that includes multiple HPC systems, petascale storage, and custom application servers. Apply online at UW Hires for req number 61505.  http://www.washington.edu/admin/hr/jobs/

Loading...

For reprints and/or copyright permission, please contact The YGS Group, 3650 West Market Street, York, PA;

(717) 505-9701 ext. 125, or via email to Ashley.Zander@theYGSgroup.com.