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Interoperability Perspectives and Insights from the eHealth Exchange Annual Meeting

Healthcare IT Today

This week I had a chance to attend the eHealth Exchange Annual meeting to learn more about what’s happening with their network along with a wide variety of inteorperability topics. The conference covered a wide range of topics from public health to TEFCA and everything in between. Lots of things to still figure out.

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Agency heads pitch Congress on public health data

Morning eHealth

HHS unveils unified agenda — FDA's PDF hopes

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TEFCA Is Live – Clarifying Common Misperceptions

Healthcare IT Today

The following is a guest article by Jay Nakashima, President at eHealth Exchange Change is scary. At eHealth Exchange, which is one of the first Qualified Health Information Networks™ (QHINs™) under TEFCA, we have a front-row seat to the framework’s ongoing implementation. But we believe that is a mistake.

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A call to upgrade public health data

Morning eHealth

The latest on CMS’ AI challenge — Study finds about one in 10 Instagram posts advertising drug sales

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The Balance Between Promoting Data Sharing and Ensuring the Privacy and Security of Sensitive Health Information

Healthcare IT Today

While that may not affect an individual patient whose data is included in the data set, it affects patient outcomes overall because it allows us to analyze the data and provide early interventions and programs. Jay Nakashima, President at eHealth Exchange Keeping patient data safe and private is our top priority.

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Big ONC News: QHINs, TEFCA, and HTI-1

Healthcare IT Today

This is a big step forward for QHINs who can now start sharing health data. HTI-1 Final Rule Appropriately, we’ve been breaking down what health IT and EHR vendors need to expect when it comes to HTI-1 in our Healthcare Regulatory Talk series.

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Not All QHINs Will Be Created Equal

Healthcare IT Today

The following is a guest article by Jay Nakashima, Executive Director at eHealth Exchange. For the health IT community, 2022 has been a big year. . Currently, perhaps 99% of health data exchange is initiated to support treatment. Does the Exchange Allow Participants Full Control Over Their Data?

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