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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.

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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 Comments Submitted RE: ICD-10 Delay

May 17, 2012

Re: 45 CFR Part 162 [CMS–0040–P] RIN 0938–AQ13Administrative Simplification: Adoption of a Standard for a Unique Health Plan Identifier; Addition to the National Provider Identifier Requirements; and a Change to the Compliance Date for ICD–10–CM and ICD–10–PCS Medical Data Code Sets

AMIA Comments on PCORI Draft Research Agenda

March 16, 2012

AMIA and the NIWG submitted comments in response to the Patient-Centered Outcomes Research Institute’s (PCORI’s) request for comments about its draft National Priorities for Research and Research Agenda. PCORI was created to fund research that will give patients, caregivers, and clinicians more information to support health care decisions. AMIA thanked […]