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AMIA’s goal is to improve the legislative and regulatory environment for health informatics research, practice and education through AMIA member expertise.  The primary pathway through which AMIA achieves this goal is by engaging Federal Agencies and Congress on public calls for input, such as Notices of Proposed Rulemakings (NPRMs) or Request for Information (RFIs).

Learn more about the comment process

AMIA responses are arranged by Federal Agency and Congressional Committee.

Showing 11 - 20 out of 22

Food and Drug Administration Safety and Innovation Act (FDASIA)

July 7, 2014

AMIA Comments on Proposed Risk-Based Regulatory Framework and Strategy for Health Information Technology Report

On behalf of the American Medical Informatics Association (AMIA), I am pleased to submit these comments in response to the above-referenced request. AMIA is the professional home for biomedical and health informatics and is dedicated to […]

AMIA participates in Coalition for an Informed Patient Identity Integrity Solution

November 29, 2011

Along with several other organizations, AMIA is participating in the Coalition for an Informed Patient Identity Integrity Solution. The Coalition is working to delete prohibiting language from the fiscal year 2012 Labor, HHS Appropriations bill, and to substitute language that would have HHS conduct a study of the health information […]

AMIA Testifies before ONC's Privacy & Security Tiger Team

December 9, 2010

AMIA’s testimony examines patient data matching before ONC’s Privacy & Security Tiger Team. AMIA's Brad Malin discusses some concerns of the accuracy in patient matching and the implications of misidentified data in patient care and biomedical research, which could lead to false match or false non-match.

Letter to Chairman Stark regarding HR 1467

September 18, 2008

Joint AMIA/AHIMA letter to Chairman Stark regarding including provisions of HR 1467, the "10,000 Trained by 2010 Act," in HR 6898, the "Health-e Information Technology Act."