{"id":87295,"date":"2025-04-22T10:00:53","date_gmt":"2025-04-22T15:00:53","guid":{"rendered":"https:\/\/osteopathic.org\/?p=87295"},"modified":"2025-04-16T16:00:49","modified_gmt":"2025-04-16T21:00:49","slug":"aoa-weighs-in-on-fdas-ai-device-guidance","status":"publish","type":"post","link":"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/","title":{"rendered":"AOA weighs in on FDA\u2019s AI device guidance"},"content":{"rendered":"<p>The AOA <a href=\"https:\/\/osteopathic.org\/index.php?aam-media=\/wp-content\/uploads\/AOA-Comment-FDA-AI-TPLC-Guidance-Comments.pdf\" target=\"_blank\" rel=\"noopener\">submitted comments<\/a> to the FDA on its proposed guidance for marketing submissions of artificial intelligence (AI)-enabled medical devices. The AOA supports the FDA\u2019s efforts to promote innovation and improve patient care through AI but urges stronger safeguards to ensure transparency, reduce bias and protect patients.<\/p>\n<p>Key recommendations include making several voluntary guidance elements\u2014such as detailed device descriptions, risk assessments and data management protocols\u2014mandatory. The AOA calls for clearer labeling that discloses the data used to train AI tools, including demographics and geographic scope, to help physicians assess appropriateness for their patient populations.<\/p>\n<p>The AOA also encourages the FDA to strengthen validation and post-market monitoring requirements, noting that bias and underperformance often emerge after deployment. Without adequate oversight, state-level patchwork regulation could increase costs and hinder innovation. To foster trust and adoption, the AOA <a href=\"https:\/\/osteopathic.org\/index.php?aam-media=\/wp-content\/uploads\/AOA-Comment-FDA-AI-TPLC-Guidance-Comments.pdf\" target=\"_blank\" rel=\"noopener\">advocates<\/a> for improved transparency, equity and performance standards throughout the AI device lifecycle. The AOA remains committed to collaborating with the FDA to ensure safe, reliable AI integration in health care.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The AOA submitted comments to the FDA on its proposed guidance for marketing submissions of artificial intelligence (AI)-enabled medical devices. The AOA supports the FDA\u2019s efforts to promote innovation and improve patient care through AI but urges stronger safeguards to ensure transparency, reduce bias and protect patients. Key recommendations include making several voluntary guidance elements\u2014such &hellip; <a href=\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/\" class=\"readmore\">Read More<\/a><\/p>\n","protected":false},"author":52605,"featured_media":83944,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[7013],"tags":[],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v21.4 (Yoast SEO v21.4) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>AOA weighs in on FDA\u2019s AI device guidance - American Osteopathic Association<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"AOA weighs in on FDA\u2019s AI device guidance\" \/>\n<meta property=\"og:description\" content=\"The AOA submitted comments to the FDA on its proposed guidance for marketing submissions of artificial intelligence (AI)-enabled medical devices. 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Key recommendations include making several voluntary guidance elements\u2014such &hellip; Read More\" \/>\n<meta property=\"og:url\" content=\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/\" \/>\n<meta property=\"og:site_name\" content=\"American Osteopathic Association\" \/>\n<meta property=\"article:published_time\" content=\"2025-04-22T15:00:53+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-04-16T21:00:49+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/osteopathic.org\/wp-content\/uploads\/AI-webinar.png\" \/>\n\t<meta property=\"og:image:width\" content=\"480\" \/>\n\t<meta property=\"og:image:height\" content=\"320\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Katie Arvia\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Katie Arvia\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/\",\"url\":\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/\",\"name\":\"AOA weighs in on FDA\u2019s AI device guidance - American Osteopathic Association\",\"isPartOf\":{\"@id\":\"https:\/\/osteopathic.org\/#website\"},\"datePublished\":\"2025-04-22T15:00:53+00:00\",\"dateModified\":\"2025-04-16T21:00:49+00:00\",\"author\":{\"@id\":\"https:\/\/osteopathic.org\/#\/schema\/person\/1e0b92da0113c23316ae94ea235ce965\"},\"breadcrumb\":{\"@id\":\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/osteopathic.org\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"AOA weighs in on FDA\u2019s AI device guidance\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/osteopathic.org\/#website\",\"url\":\"https:\/\/osteopathic.org\/\",\"name\":\"American Osteopathic Association\",\"description\":\"Advancing the distinctive philosophy and practice of osteopathic medicine\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/osteopathic.org\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/osteopathic.org\/#\/schema\/person\/1e0b92da0113c23316ae94ea235ce965\",\"name\":\"Katie Arvia\",\"url\":\"https:\/\/osteopathic.org\/author\/460084\/\"}]}<\/script>\n<!-- \/ Yoast SEO Premium plugin. -->","yoast_head_json":{"title":"AOA weighs in on FDA\u2019s AI device guidance - American Osteopathic Association","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/osteopathic.org\/2025\/04\/22\/aoa-weighs-in-on-fdas-ai-device-guidance\/","og_locale":"en_US","og_type":"article","og_title":"AOA weighs in on FDA\u2019s AI device guidance","og_description":"The AOA submitted comments to the FDA on its proposed guidance for marketing submissions of artificial intelligence (AI)-enabled medical devices. 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