The public will get a chance to comment on a proposed risk-based regulatory framework for health information technology developed by the Food and Drug Administration in coordination with the Office of the National Coordinator for Health IT and Federal Communications Commission. 

In an April 7 Federal Register notice, the FDA announced the availability of the draft report and website location where it can be downloaded as well as a docket where stakeholders may provide comments. The public has until July 7 to submit comments either electronically or in writing.

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