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12:00 AM - 29th ECCMID
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29th ECCMID
2019-04-13 - 2019-04-16    
All Day
Welcome to ECCMID 2019! We invite you to the 29th European Congress of Clinical Microbiology & Infectious Diseases, which will take place in Amsterdam, Netherlands, [...]
4th International Conference on  General Practice & Primary Care
2019-04-15 - 2019-04-16    
All Day
The 4th International Conference on General Practice & Primary Care going to be held at April 15-16, 2019 Berlin, Germany. Designation Statement The theme of [...]
Digital Health Conference 2019
2019-04-24 - 2019-04-25    
12:00 am
An Innovative Bridging for Modern Healthcare About Hosting Organization: conference series llc ltd |Conference Series llc ltd Houston USA| April 24-25,2019 Conference series llc ltd, [...]
International Conference on  Digital Health
2019-04-24 - 2019-04-25    
All Day
Details of Digital Health 2019 conference in USA : Conference Name                              [...]
16th Annual World Health Care Congress -WHCC19
2019-04-28 - 2019-05-01    
All Day
16th Annual World Health Care Congress will be organized during April 28 - May 1, 2019 at Washington, DC Who Attends Hospitals, Health Systems, & [...]
Events on 2019-04-13
29th ECCMID
13 Apr 19
Amsterdam
Events on 2019-04-24
Events on 2019-04-28
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