Thursday, September 19, 2013

Health IT Likely Subject to FDA Regulation

On September 4, 2013, subgroup members of the National Coordinator for Health IT HIT Policy Committee discussed the Health IT most likely to be subject to Food and Drug Administration (FDA) regulation.

Technology likely to be in the risk-based framework being developed include electronic health records (EHRs) and health information exchange (HIE) software.

"National Coordinator for Health IT's HIT Policy Committee, members of a subgroup discussed the health IT likely to be subject to Food and Drug Administration regulation in the near future."
- Becker Hospital Review
Both EHRs and HIEs are at risk for patient privacy data breaches. To proactively detect such breaches, healthcare organizations are utilizing low-cost on-demand SaaS analytics services.
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(a) The Health IT Most Likely to be Subjected to FDA Regulation -, 09/05/2013

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