{"id":87696,"date":"2026-06-27T02:14:21","date_gmt":"2026-06-27T02:14:21","guid":{"rendered":"https:\/\/www.europesays.com\/ai\/87696\/"},"modified":"2026-06-27T02:14:21","modified_gmt":"2026-06-27T02:14:21","slug":"hhs-identifies-three-priorities-for-clinical-ai-adoption","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ai\/87696\/","title":{"rendered":"HHS Identifies Three Priorities for Clinical AI Adoption"},"content":{"rendered":"<p>Officials outlined efforts for implementation support, coordination and evaluation standards with new AI regulatory proposals expected soon.<\/p>\n<p>Federal health officials outlined three priorities Thursday that they said will accelerate <a href=\"https:\/\/govciomedia.com\/from-fax-machines-to-ai-health-agencies-accelerate-modernization\/\" rel=\"nofollow noopener\" target=\"_blank\">artificial intelligence adoption in clinical care<\/a>, focusing on better agency coordination, implementation guidance and clearer standards for evaluating AI tools.<\/p>\n<p>Officials said those goals will shape future department actions as it implements AI.\u00a0<\/p>\n<p>\u201cWe believe that starting with these three things and acting on constant engagement from this community is what\u2019s needed to establish trust,\u201d said HHS Deputy Chief AI Officer Arman Sharma. \u201cAnd trust in this technology is the only thing that will lead to responsible but also effective adoption.\u201d\u00a0<\/p>\n<p>Thomas Keane, <a href=\"https:\/\/govciomedia.com\/hhs-restores-onc-keeps-key-health-it-programs-intact\/\" rel=\"nofollow noopener\" target=\"_blank\">national coordinator for Health IT<\/a>,\u00a0said AI is already reducing administrative work, helping enroll patients in clinical trials, accelerating drug discovery and giving patients better access to health information.<\/p>\n<p>\u201cMost importantly, it\u2019s empowering patients to understand and take control of their own health,\u201d Keane said.\u00a0<\/p>\n<p>7,000 Public Comments Shaped the Strategy<\/p>\n<p>The Department of Health and Human Services identified the three priorities from the more than 7,000 comments submitted in response to a <a href=\"https:\/\/www.federalregister.gov\/documents\/2025\/12\/23\/2025-23641\/request-for-information-accelerating-the-adoption-and-use-of-artificial-intelligence-as-part-of\" rel=\"nofollow noopener\" target=\"_blank\">December request for information<\/a> (RFI). <\/p>\n<p>The RFI came as part of the Trump administration\u2019s effort to accelerate clinical AI adoption across healthcare. Rather than focusing solely on AI development, the department sought recommendations on how to use its regulatory, reimbursement, and research and development authorities to speed implementation of AI technologies in clinical care.\u00a0<\/p>\n<p>The department specifically requested feedback on modernizing digital health regulation, aligning reimbursement with AI-enabled care, supporting implementation research, reducing provider burden, improving patient outcomes and lowering healthcare costs. Officials said the RFI was intended to extend HHS\u2019s internal AI strategy into a broader, department-wide effort to encourage AI adoption across the healthcare system.\u00a0<\/p>\n<p>Adoption, Not Just Innovation\u00a0<\/p>\n<p>A common theme in the public comments was the need for adoption support, according to Sharma. Building AI tools is only one part of the challenge, he said. Providers also need governance frameworks, implementation guidance and confidence that products have been adequately evaluated.\u00a0<\/p>\n<p>\u201cWe recognize that even with the most agile regulation, even with optimal reimbursement, there\u2019s still an implementation gap,\u201d Sharma said. \u201cThere\u2019s still process and workflow optimization that\u2019s required to take AI and bring it into existing workflows within any care setting, whether that be a small clinic or whether that be a large academic medical center.\u201d\u00a0<\/p>\n<p>Sharma pointed to ARPA-H as an agency working to accelerate AI adoption in clinical care. Its Agentic AI-EnableD CardioVascular CAre TransfOrmation (ADVOCATE) program\u00a0would be the first of its kind, FDA-approved clinical agentic AI system. Its goal is to \u201ctransform advanced cardiovascular disease management with an agentic AI system that can provide 24\/7 holistic clinical care.\u201d \u00a0\u00a0<\/p>\n<p>ARPA-H program manager and cardiologist Haider Warraich said the vision is for ADVOCATE to do everything a clinician can over the phone.\u00a0<\/p>\n<p>\u201cThat could include administrative functions, such as helping set up appointments, helping provide advice about diet and lifestyle, which is so important for patients with cardiovascular disease, but also provide actual diagnoses, perform actual triage, and really perform high-risk functions, including being able to change medications or prescribe new medications,\u201d he said.\u00a0<\/p>\n<p>Warraich acknowledged concerns about introducing powerful technology and said he supported building a \u201csupervisory layer\u201d that would optimize human oversight of the technologies after they\u2019ve been deployed in the postmarket. He also said implementing the program is \u201cgoing to be incredibly challenging\u201d and welcomed health systems to co-develop the technology and then deploy it in their clinical settings in randomized clinical trials.\u00a0<\/p>\n<p>FDA Prepares Updated AI Policy\u00a0<\/p>\n<p>Rick Abramson, director of the Food and Drug Administration\u2019s Digital Health Center of Excellence, said the agency plans to release new policy ideas for stakeholder comment as it updates its regulatory approach to increasingly sophisticated <a href=\"https:\/\/govciomedia.com\/cms-fda-launch-pilot-programs-to-modernize-digital-health-for-medicare\/\" rel=\"nofollow noopener\" target=\"_blank\">AI-enabled medical devices<\/a>.\u00a0<\/p>\n<p>Abramson avoided discussing specific proposals because of ongoing policy development, but outlined several themes expected to guide future oversight. He said the FDA plans to address four areas that the public has consistently requested, including:\u00a0<\/p>\n<p>Greater\u00a0clarity on what the FDA regulates, what is required of sponsors and what role FDA will play in both the premarket and post market settings.\u00a0<\/p>\n<p>Oversight proportional to risk.\u00a0<\/p>\n<p>Appropriate oversight across the\u00a0lifecycle of AI products after they enter the market.\u00a0<\/p>\n<p>The need for policy coordination among federal agencies, between federal and state oversight bodies and also with international regulators.\u00a0<\/p>\n<p>He noted that AI technologies evolve much faster than traditional regulatory frameworks, requiring the FDA to continuously adapt its approach as both the technology and clinician interaction with AI change.\u00a0<\/p>\n<p>\u201cThe world is looking to the FDA for leadership in how to approach advanced clinical AI tools. We plan to meet the challenge, and the public should be expecting us to release some ideas to the public for stakeholder comment in very short order,\u201d he said. \u00a0<\/p>\n","protected":false},"excerpt":{"rendered":"Officials outlined efforts for implementation support, coordination and evaluation standards with new AI regulatory proposals expected soon. Federal&hellip;\n","protected":false},"author":2,"featured_media":87697,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[24,25,19539,34385,21903],"class_list":["post-87696","post","type-post","status-publish","format-standard","has-post-thumbnail","category-ai","tag-ai","tag-artificial-intelligence","tag-fda","tag-health-it","tag-hhs"],"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/posts\/87696","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/comments?post=87696"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/posts\/87696\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/media\/87697"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/media?parent=87696"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/categories?post=87696"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ai\/wp-json\/wp\/v2\/tags?post=87696"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}