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.
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 submitted comments recently to the National Institute of Nursing Research (NINR) in response to their request for public comments on the latest draft of the Institute's strategic plan. The association's comments were informed by AMIA's Nursing Informatics Working Group (NIWG), which promotes the advancement of nursing informatics within the […]
Re: Request for Information Regarding the President’s Council of Advisors on Science and Technology (PCAST) Report Entitled "Realizing the Full Potential of Health Information Technology to Improve Healthcare for Americans: The Path Forward"
Dear Mr. Posnack,
On behalf of AMIA, I am pleased to submit these comments regarding the recently […]
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 […]
AMIA comments on the proposed rule which implements the initial stage of incentive funding for meaningful use (MU) of certified EHR technology. AMIA strongly believes that three principles are essential to achieving meaningful use of certified EHR technology: 1) we must invest in people, as well as technology; 2) users […]
AMIA’s testimony to the HIT Policy Committee, Adoption/Certification Workgroup, discusses potential unintended consequences of health information technology (HIT) and HIT policy, as well as effective options for addressing them. AMIA and its task force offer several recommendations that involve unintended consequences and conjure questions from previous observations in identifying safety […]
AMIA NIWG submits statement to the Institute of Medicine (IOM) and the Robert Wood Johnson Foundation Initiative on the future of nursing. NIWG recognizes the importance of increasing the nursing workforce and to prepare them to meet the educational challenges of implementing HIT on a grand scale. They embrace several […]
Summary Position on Adoption of ICD-10 (pdf)- a joint statement with the American Health Information Management Association (AHIMA).