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.
In response to the U.S. Food and Drug Administration (FDA) invitation AMIA participated in a public workshop on the FDA’s Draft Guidance on mobile medical applications. AMIA, the association for informatics professionals, made a presentation and participated in panel discussions that advised the FDA on how it should approach its […]
AMIA President and CEO Ted Shortliffe sent a letter today to ONC director Farzad Mostashari and the leadership of all Regional Extension Centers (RECs) regarding a recent AMIA Board position paper on vendor agreements. Click below for a PDF copy of the letter.
AMIA submitted comments today on the proposed rule from the Centers for Medicare and Medicaid Services (CMS) on the Medicare Shared Savings Program: Accountable Care Organizations (ACOs).
In the comments, AMIA president Ted Shortliffe asserts that ACOs, especially as enabled by the science of biomedical and health informatics and tools […]
Today, AMIA and its Nursing Informatics Working Group provided input to National Quality Forum (NQF) during an open comment period to solicit input on NQF's Quality Data Model (QDM). The QDM provides a way to describe clinical concepts in a standardized format so that those monitoring clinical performance and outcomes […]
AMIA has weighed in on the Federal Health IT Strategic Plan in response to the HHS Office of the National Coordinator’s (ONC) call for comments on the overarching strategy for realizing health IT goals set forth by the U.S. Congress and the Administration. AMIA states in its comments to ONC […]
Dear eMeasure Format Review Panel:
On behalf of AMIA (the American Medical Informatics Association), we are pleased to submit these comments to help inform your important discussions. AMIA is an unbiased, authoritative source within the informatics community and the healthcare industry. AMIA and its members are transforming health care through […]
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.
AMIA submitted comments to HHS on the Common Format, Device or Medical/Surgical Supply, including HIT Devices. The comments address patient safety data collections and event reporting. Failures with HIT devices are different from those associated with other devices and warrant a distinct form and classification for reporting failures. AMIA submits […]
The current commercial health information technology (IT) arena encompasses a number of competing firms that provide electronic health applications to hospitals, clinical practices, and other healthcare-related entities. Such applications collect, store, and analyze patient information. Some vendors incorporate contract language whereby purchasers of health IT systems, such as hospitals and […]
AMIA comments to DEA on E-Prescribing Controlled Substances which would revise the Comprehensive Drug Abuse Prevention and Control Act of 1970 (Controlled Substances Act, or CSA) and the related regulations to allow healthcare providers to write prescriptions for controlled substances electronically. These revisions would have to allow e-prescribing controlled substances […]