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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).

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AMIA responses are arranged by Federal Agency and Congressional Committee.

Showing 11 - 20 out of 63

AMIA Supports, Encourages Further Refinement of FDA AI/Machine Learning Regulatory Framework

June 5, 2019

In comments submitted this week to the U.S. Food and Drug Administration (FDA), the nation’s informatics professionals applauded the agency for developing a regulatory Modification Framework for Artificial Intelligence (AI)/Machine Learning (ML)-based software as a medical device (SaMD). The American Medical Informatics Association (AMIA) offered additional observations and recommendations for […]

AMIA Calls on HHS to Decouple Clinical Documentation and Administrative Requirements

January 29, 2019

In comments submitted to ONC and CMS, AMIA recommended that the Department of Health and Human Services orient its documentation burden reduction strategy towards a long-term goal of decoupling clinical documentation from billing, regulatory, and administrative compliance requirements. AMIA highlighted the unique opportunity to leverage informatics tools and methodologies to […]

AMIA Supports National Testing Collaborative for Health IT

December 20, 2018

In response to a Request for Information from the Centers for Disease Control and Prevention, AMIA urged HHS officials to focus on narrow use cases, such as CDS or eCQMs, when conceptualizing a national collaborative for health IT testing. AMIA also outlined the pros/cons of focusing on CDS versus eCQMs […]

AMIA Supports CMS Efforts to Reduce Documentation Burden, Streamline MIPS

September 10, 2018

In response to the CMS CY2019 Physician Fee Schedule NPRM, AMIA applauded federal officials for aligning physician and hospital EHR requirements and advancing policies that further incentivize the adoption of health IT for patient care. AMIA also supported CMS efforts to reduce documentation burden through new options to use time […]

AMIA Provides FDA Lit Review on Risk and Benefits of Medical Software

June 28, 2018

AMIA responded to an FDA request for input with a preliminary review of relevant research into the specific benefits and risks to health associated with software functions that the 21st Century Cures Act excluded from the definition of medical device. While some health IT applications to healthcare delivery have unambiguously […]

AMIA and Pew Letter to ONC on 21st Century Cures EHR Reporting Measures

December 14, 2017

Under the 21st Century Cures Act, the Office of the National Coordinator for Health IT (ONC) is supposed to implement an EHR reporting program. However, recent budget proposals would cut ONC’s funding – something ONC officials have said would prevent them from fully implementing this safety provision. The Cures Act […]