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San Jose Health IT Summit
2017-04-13 - 2017-04-14    
All Day
About Health IT Summits U.S. healthcare is at an inflection point right now, as policy mandates and internal healthcare system reform begin to take hold, [...]
Annual IHI Summit
2017-04-20 - 2017-04-22    
All Day
The Office Practice & Community Improvement Conference ​​​​​​The 18th Annual Summit on Improving Patient Care in the Office Practice and the Community taking place April 20–22, 2017, in Orlando, FL, brings together 1,000 health improvers from around the globe, in [...]
Stanford Medicine X | ED
2017-04-22 - 2017-04-23    
All Day
Stanford Medicine X | ED is a conference on the future of medical education at the intersections of people, technology and design. As an Everyone [...]
2017 Health Datapalooza
2017-04-27 - 2017-04-28    
All Day
Health Datapalooza brings together a diverse audience of over 1,600 people from the public and private sectors to learn how health and health care can [...]
The 14th Annual World Health Care Congress
2017-04-30 - 2017-05-03    
All Day
The 14th Annual World Health Care Congress April 30 - May 3, 2017 • Washington, DC • The Marriott Wardman Park Hotel Connecting and Preparing [...]
Events on 2017-04-13
San Jose Health IT Summit
13 Apr 17
San Jose
Events on 2017-04-20
Annual IHI Summit
20 Apr 17
Orlando
Events on 2017-04-22
Events on 2017-04-27
2017 Health Datapalooza
27 Apr 17
Washington, D.C
Events on 2017-04-30
Articles

Nov 09: EHR Association backs no FDA regulation for EHR systems

repair health portal

The Electronic Health Record Association, which represents 40 EHR developer companies whose products are in use at a majority of hospitals and physician practices today, applauds an FDA regulation workgroup recommendation that healthcare technology, such as EHR systems, should not be treated as medical devices and should remain unregulated.

However, the group, in a Nov. 6 letter to HHS Secretary Kathleen Sebelius, asked for clarification on a number of topics, including clinical decision support, medical device accessories, reporting of safety event and post-market surveillance and “Class 0.”

“We are not convinced that most HIT not regulated as a medical device should receive a new ‘Class 0’ device classification by the FDA. Such a classification and application for a formal regulatory approach to HIT is not warranted in our view,” stated the letter signed by the EHR Association Executive Committee members, whose chair is Michele McGlynn, senior director, strategy and operations at Siemens.

The Association recommended the following:

  • Any definition of HIT used in a new risk-based policy framework should align with existing market definitions. The focus should be on what specific types of HIT are subject to which types of regulation or oversight, if any.
  •  A patient safety risk framework and examples should be used as building blocks to develop a robust and transparent plan that that would allow application of oversight by level of risk and associated costs and benefits of oversight. Any such framework must include weights for risk elements and a model to combine results.
  • To the extent that enforcement discretion is used, it should be used in a manner that creates greater predictability as opposed to regulatory uncertainty, with enforcement discretion identified as the clear outcome of a considered policy process and one that can be expected to remain in place for some time. We believe that the approach taken related to the recent FDA guidance on mobile devices is a good example of providing useful guidance and minimizing uncertainty, while allowing the framework and the market to evolve. As a general proposition, we urge that any deliberations regarding increased oversight of HIT be conducted in ways that increase predictability and certainty for developers and providers.  source