{
  "legislationId": "118_S_4862",
  "lastUpdate": "2026-02-10T19:55:38.787Z",
  "history": [
    {
      "timestamp": "2026-02-10T19:55:38.787Z",
      "source_url": "https://www.congress.gov/118/bills/s4862/BILLS-118s4862is.htm",
      "model": "gemini-3-pro-preview",
      "prompt_sent": "\nJesteś LEGISLATIVE SURGEON.\nTwoim zadaniem jest audyt i naprawa streszczenia (JSON) pod kątem zgodności z tekstem źródłowym (SOURCE).\nZASADA FUNDAMENTALNA: \"NO NEW INFORMATION\" (żadnych nowych informacji).\nStreszczenie może jedynie transformować informacje zawarte w SOURCE (skracać, tłumaczyć, sumować). Nie może generować nowych informacji, których nie ma w SOURCE.\n\nPROCEDURA WERYFIKACJI (wykonaj dla każdego zdania w JSON):\nZadaj sobie pytanie: \"Czy potrafię wskazać w SOURCE konkretny fragment, który potwierdza to stwierdzenie?\"\nJEŚLI ODPOWIEDŹ BRZMI \"TAK\":\nInformacja jest potwierdzona cytatem, synonimem lub wynikiem matematycznym z danych w tekście.\nDECYZJA: Zostaw bez zmian.\nJEŚLI ODPOWIEDŹ BRZMI \"NIE\":\nInformacji nie ma w tekście (jest to halucynacja, zewnętrzna wiedza modelu, nadinterpretacja lub niepotrzebna ekstrapolacja).\nDECYZJA: Usuń tę informację lub zmień ją tak, aby miała pokrycie w tekście.\nJEŚLI ODPOWIEDŹ BRZMI \"TO ZALEŻY\":\nTekst jest niejasny, a streszczenie \"zgaduje\" (np. podając konkretny przykład dla ogólnego terminu).\nDECYZJA: Bądź bezpieczny. Usuń zgadywanie. Użyj terminologii z tekstu.\n\nKATEGORIE RYZYKA (szczególna uwaga):\nDaty (start obowiązywania vs start finansowania).\nLiczby (konkretne kwoty muszą wynikać z tekstu).\nPodmioty (kto co robi).\nZakres (co ustawa obejmuje, a czego nie).\n\nINPUT:\n--- SOURCE_TEXT START ---\n[Congressional Bills 118th Congress] [From the U.S. Government Publishing Office] [S. 4862 Introduced in Senate (IS)] <DOC> 118th CONGRESS 2d Session S. 4862 To ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes. _______________________________________________________________________ IN THE SENATE OF THE UNITED STATES July 30, 2024 Mr. Rounds (for himself and Mr. Heinrich) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and Pensions _______________________________________________________________________ A BILL To ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes. Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1. GOVERNING ETHICAL AI USE AND INNOVATION FOR HEALTH CARE DEVELOPMENT. (a) National Institutes of Health.--Part A of title IV of the Public Health Service Act is amended by inserting after section 403D (42 U.S.C. 283a-3) the following: ``SEC. 403E. ARTIFICIAL INTELLIGENCE. ``(a) In General.--The Director of NIH shall-- ``(1) develop computational resources and datasets necessary to use artificial intelligence approaches for health and health care research; ``(2) provide expertise in biomedical research and the use of artificial intelligence; ``(3) develop and maintain federated resources that provide unified access to data from fundamental biomedical research and the clinical care environment; ``(4) provide education and ongoing support to a nationwide user community to foster scientifically sound, ethical, and inclusive research using artificial intelligence that addresses the health needs of all individuals; and ``(5) extend the clinical research capabilities of the National Institutes of Health to address significant gaps in evidence to guide clinical care and to serve the needs of every community. ``(b) Authorization of Appropriations.--There is authorized to be appropriated to the Director of NIH to carry out this section $400,000,000 for fiscal year 2025.''. (b) Office of the National Coordinator for Health Information Technology.--Subtitle C of title XXX of the Public Health Service Act (42 U.S.C. 300jj-51 et seq.) is amended by adding at the end the following: ``SEC. 3023. ARTIFICIAL INTELLIGENCE. ``(a) In General.--The National Coordinator shall-- ``(1) carry out activities to engage in health research by-- ``(A) utilizing the electronic health record as a data collection tool; and ``(B) requiring that individuals are offered an opportunity to direct the use of their health data for health care research; and ``(2) establish data and interoperability standards for access, exchange, and use of clinical and administrative data from the clinical care environment through a National Artificial Intelligence Research Resource, in alignment with-- ``(A) the United States Core Data for Interoperability; ``(B) the Fast Health Interoperability Resources; and ``(C) the Trusted Exchange Framework and Common Agreement. ``(b) Authorization of Appropriations.--There are authorized to be appropriated to the National Coordinator for fiscal year 2025-- ``(1) $10,000,000 to carry out subsection (a)(1); and ``(2) $50,000,000 to carry out subsection (a)(2).''. (c) Medicare Requirement for Hospitals Relating to Use of Electronic Health Records Data for Biomedical Research Purposes.-- Section 1866(a)(1) of the Social Security Act (42 U.S.C. 1395cc(a)(1)) is amended-- (1) by moving the indentation of subparagraph (W) 2 ems to the left; (2) in subparagraph (X)-- (A) by moving the indentation 2 ems to the left; and (B) by striking ``and'' at the end; (3) in subparagraph (Y), by striking the period at the end and inserting ``; and''; and (4) by inserting after subparagraph (Y) the following new subparagraph: ``(Z) in the case of a hospital, with respect to each individual who is admitted to the hospital on or after the date that is 1 year after the date of enactment of this subparagraph, to-- ``(i) request permission of the individual to share the health data of the individual for health-related research purposes in accordance with section 3023(a)(1) of the Public Health Service Act; and ``(ii) in the case where the individual grants permission to the sharing of such data, share the electronic health record of the individual for such purposes in accordance with such section.''. (d) Sense of the Senate.--It is the sense of the Senate that any steering subcommittee (or similar entity) for a National Artificial Intelligence Research Resource established in the Interagency Committee established under section 5103 of the William M. (Mac) Thornberry National Defense Authorization Act for Fiscal Year 2021 (15 U.S.C. 9413) shall include an officer or employee of the National Institutes of Health. (e) National Library of Medicine.-- (1) In general.--Section 465(b) of the Public Health Service Act (42 U.S.C. 286(b)) is amended-- (A) in paragraph (7), by striking ``and'' after the semicolon; (B) by redesignating paragraph (8) as paragraph (10); and (C) by inserting after paragraph (7) the following: ``(8) establish facilities so that the Library serves as the central exchange center of federated data sharing; ``(9) establish a core data science program to guide and enable a diverse and comprehensive community of health-related research data users; and''. (2) Authorization of appropriations.--Subpart 1 of part D of title IV of the Public Health Service Act (42 U.S.C. 286 et seq.) is amended by adding at the end the following: ``SEC. 468. AUTHORIZATION OF APPROPRIATIONS. ``There are authorized to be appropriated to the Secretary for fiscal year 2025-- ``(1) $100,000,000 to carry out section 465(b)(8); and ``(2) $100,000,000 to carry out section 465(b)(9).''. <all>\n--- SOURCE_TEXT END ---\n\n--- FLAGGED_JSON START ---\n{\n  \"pl_ai_title\": \"Etyczne wykorzystanie sztucznej inteligencji w badaniach medycznych i opiece zdrowotnej.\",\n  \"pl_summary\": \"Ustawa przeznacza setki milionów dolarów na rozwój sztucznej inteligencji w służbie zdrowia, mając na celu poprawę opieki medycznej i przyspieszenie badań. Kluczową zmianą dla obywateli jest wprowadzenie obowiązku pytania pacjentów przez szpitale o zgodę na wykorzystanie ich elektronicznej dokumentacji medycznej w celach badawczych. Ma to zapewnić etyczne i kontrolowane wykorzystanie danych do tworzenia nowych narzędzi diagnostycznych i leczniczych.\",\n  \"pl_key_points\": [\n    \"Szpitale uczestniczące w programie Medicare będą musiały prosić pacjentów o zgodę na udostępnianie ich elektronicznej dokumentacji medycznej (EHR) do celów badawczych.\",\n    \"Powstają nowe, ujednolicone zasoby danych na poziomie krajowym, zarządzane przez NIH i ONC, aby przyspieszyć rozwój etycznej sztucznej inteligencji w medycynie.\",\n    \"Autoryzowano przeznaczenie 660 milionów dolarów na rok fiskalny 2025 na finansowanie tych działań, w tym na tworzenie zasobów obliczeniowych i edukację w zakresie AI.\"\n  ],\n  \"eng_ai_title\": \"Ethical AI Adoption in Healthcare: Data Consent and Research Funding.\",\n  \"eng_summary\": \"This bill authorizes significant funding to accelerate the ethical development of Artificial Intelligence in healthcare, aiming to improve medical treatment and research nationwide. Crucially, it establishes new rules requiring hospitals to ask patients for permission before sharing their electronic health records for AI research purposes. This ensures individuals maintain control over how their personal health data is utilized for scientific advancement.\",\n  \"eng_key_points\": [\n    \"Hospitals participating in Medicare must request patient permission to share Electronic Health Records (EHR) data for health-related research.\",\n    \"The law authorizes $660 million for Fiscal Year 2025 to fund federal agencies (NIH, ONC, NLM) to develop AI research resources and data standards.\",\n    \"New national data resources and interoperability standards will be established to unify access to clinical data for ethical biomedical AI research.\"\n  ],\n  \"de_ai_title\": \"Ethische KI im Gesundheitswesen: Patientenzustimmung und Forschungsförderung.\",\n  \"de_summary\": \"Dieses Gesetz genehmigt erhebliche Mittel, um die ethische Entwicklung der Künstlichen Intelligenz im Gesundheitswesen zu beschleunigen und die medizinische Versorgung zu verbessern. Eine wichtige Änderung ist die Verpflichtung für Krankenhäuser, Patienten um Erlaubnis zu bitten, bevor ihre elektronischen Gesundheitsdaten für KI-Forschungszwecke weitergegeben werden. Dies stärkt die Kontrolle der Bürger über ihre persönlichen Gesundheitsdaten.\",\n  \"de_key_points\": [\n    \"Krankenhäuser, die am Medicare-Programm teilnehmen, müssen Patienten um Erlaubnis bitten, ihre elektronischen Gesundheitsakten (EHR) für Forschungszwecke zu teilen.\",\n    \"Es werden 660 Millionen Dollar für das Geschäftsjahr 2025 bereitgestellt, um Bundesbehörden (NIH, ONC) bei der Entwicklung von KI-Forschungsressourcen und Datenstandards zu unterstützen.\",\n    \"Es werden neue nationale Datenressourcen und Interoperabilitätsstandards geschaffen, um den Zugang zu klinischen Daten für ethische biomedizinische KI-Forschung zu vereinheitlichen.\"\n  ],\n  \"fr_ai_title\": \"Adoption éthique de l'IA en santé: consentement des données et financement de la recherche.\",\n  \"fr_summary\": \"Ce projet de loi autorise un financement important pour accélérer le développement éthique de l'Intelligence Artificielle dans les soins de santé, visant à améliorer le traitement médical. Un changement clé pour les citoyens est l'obligation pour les hôpitaux de demander la permission des patients avant de partager leurs dossiers de santé électroniques à des fins de recherche en IA. Cela garantit que les individus gardent le contrôle sur l'utilisation de leurs données de santé personnelles.\",\n  \"fr_key_points\": [\n    \"Les hôpitaux participant à Medicare doivent demander l'autorisation des patients pour partager leurs dossiers de santé électroniques (DSE) à des fins de recherche.\",\n    \"660 millions de dollars sont autorisés pour l'exercice 2025 afin de financer les agences fédérales (NIH, ONC) pour développer des ressources de recherche en IA et des normes de données.\",\n    \"De nouvelles ressources nationales de données et des normes d'interopérabilité seront établies pour unifier l'accès aux données cliniques pour la recherche biomédicale éthique.\"\n  ],\n  \"es_ai_title\": \"Adopción ética de IA en salud: consentimiento de datos y financiación de investigación.\",\n  \"es_summary\": \"Esta legislación autoriza una financiación sustancial para impulsar el desarrollo ético de la Inteligencia Artificial en la atención médica, con el objetivo de mejorar los tratamientos. Un cambio fundamental para los ciudadanos es que los hospitales deberán solicitar permiso a los pacientes antes de compartir sus registros de salud electrónicos para la investigación con IA. Esto asegura que las personas mantengan el control sobre cómo se utilizan sus datos personales de salud.\",\n  \"es_key_points\": [\n    \"Los hospitales que participan en Medicare deben solicitar permiso al paciente para compartir los datos de sus Registros de Salud Electrónicos (RSE) con fines de investigación.\",\n    \"Se autorizan 660 millones de dólares para el año fiscal 2025 para financiar agencias federales (NIH, ONC) en el desarrollo de recursos de investigación de IA y estándares de datos.\",\n    \"Se establecerán nuevos recursos nacionales de datos y estándares de interoperabilidad para unificar el acceso a la información clínica para la investigación biomédica ética.\"\n  ],\n  \"it_ai_title\": \"Adozione etica dell'IA nella sanità: consenso sui dati e finanziamento della ricerca.\",\n  \"it_summary\": \"Questo disegno di legge autorizza finanziamenti significativi per accelerare lo sviluppo etico dell'Intelligenza Artificiale nel settore sanitario, mirando a migliorare i trattamenti medici. Un cambiamento cruciale per i cittadini è l'obbligo per gli ospedali di chiedere il permesso ai pazienti prima di condividere le loro cartelle cliniche elettroniche per scopi di ricerca sull'IA. Ciò garantisce che gli individui mantengano il controllo sull'utilizzo dei propri dati sanitari personali.\",\n  \"it_key_points\": [\n    \"Gli ospedali che partecipano a Medicare devono richiedere il permesso del paziente per condividere i dati delle cartelle cliniche elettroniche (EHR) per scopi di ricerca sanitaria.\",\n    \"Sono autorizzati 660 milioni di dollari per l'anno fiscale 2025 per finanziare le agenzie federali (NIH, ONC) nello sviluppo di risorse di ricerca sull'IA e standard di dati.\",\n    \"Verranno istituite nuove risorse nazionali di dati e standard di interoperabilità per unificare l'accesso ai dati clinici per la ricerca biomedica etica.\"\n  ],\n  \"nl_ai_title\": \"Ethische AI in de gezondheidszorg: toestemming voor gegevens en onderzoek financiering.\",\n  \"nl_summary\": \"Dit wetsvoorstel autoriseert aanzienlijke financiering om de ethische ontwikkeling van Kunstmatige Intelligentie in de gezondheidszorg te versnellen, met als doel de medische behandeling te verbeteren. Een cruciale verandering voor burgers is de verplichting voor ziekenhuizen om patiënten om toestemming te vragen voordat hun elektronische medische dossiers worden gedeeld voor AI-onderzoek. Dit zorgt ervoor dat individuen controle behouden over hoe hun persoonlijke gezondheidsgegevens worden gebruikt.\",\n  \"nl_key_points\": [\n    \"Ziekenhuizen die deelnemen aan Medicare moeten patiënttoestemming vragen om Elektronische Gezondheidsdossiers (EGD) te delen voor gezondheidsgerelateerde onderzoeksdoeleinden.\",\n    \"Er is 660 miljoen dollar geautoriseerd voor het fiscale jaar 2025 om federale instanties (NIH, ONC) te financieren voor de ontwikkeling van AI-onderzoeksbronnen en datastandaarden.\",\n    \"Nieuwe nationale gegevensbronnen en interoperabiliteitsstandaarden zullen worden vastgesteld om de toegang tot klinische gegevens voor ethisch biomedisch AI-onderzoek te verenigen.\"\n  ],\n  \"pt_ai_title\": \"Adoção ética de IA na saúde: consentimento de dados e financiamento de pesquisa.\",\n  \"pt_summary\": \"Este projeto de lei autoriza financiamento significativo para acelerar o desenvolvimento ético da Inteligência Artificial nos cuidados de saúde, visando melhorar o tratamento médico. Uma mudança crucial para os cidadãos é a obrigação de os hospitais solicitarem permissão aos pacientes antes de partilharem os seus registos de saúde eletrónicos para fins de pesquisa de IA. Isto garante que os indivíduos mantêm o controlo sobre a utilização dos seus dados pessoais de saúde.\",\n  \"pt_key_points\": [\n    \"Os hospitais participantes no Medicare devem solicitar a permissão do paciente para partilhar dados de Registos Eletrónicos de Saúde (RES) para fins de investigação.\",\n    \"Estão autorizados 660 milhões de dólares para o ano fiscal de 2025 para financiar agências federais (NIH, ONC) no desenvolvimento de recursos de pesquisa de IA e padrões de dados.\",\n    \"Novos recursos nacionais de dados e padrões de interoperabilidade serão estabelecidos para unificar o acesso a dados clínicos para pesquisa biomédica ética.\"\n  ],\n  \"category\": [\n    \"Health\",\n    \"Informatization\"\n  ]\n}\n--- FLAGGED_JSON END ---\n\nOUTPUT:\nWyłącznie naprawiony obiekt JSON zgodny ze strukturą:\n{\n  \"pl_ai_title\": \"...\", \"pl_summary\": \"...\", \"pl_key_points\": [...],\n  \"eng_ai_title\": \"...\", \"eng_summary\": \"...\", \"eng_key_points\": [...],\n  \"de_ai_title\": \"...\", \"de_summary\": \"...\", \"de_key_points\": [...],\n  \"fr_ai_title\": \"...\", \"fr_summary\": \"...\", \"fr_key_points\": [...],\n  \"es_ai_title\": \"...\", \"es_summary\": \"...\", \"es_key_points\": [...],\n  \"it_ai_title\": \"...\", \"it_summary\": \"...\", \"it_key_points\": [...],\n  \"nl_ai_title\": \"...\", \"nl_summary\": \"...\", \"nl_key_points\": [...],\n  \"pt_ai_title\": \"...\", \"pt_summary\": \"...\", \"pt_key_points\": [...],\n  \"category\": [\"...\"]\n}\n\n",
      "ai_response_raw": "{\n  \"pl_ai_title\": \"Etyczne wykorzystanie sztucznej inteligencji w badaniach medycznych i opiece zdrowotnej\",\n  \"pl_summary\": \"Ustawa autoryzuje finansowanie rozwoju sztucznej inteligencji w służbie zdrowia, mając na celu poprawę opieki medycznej i przyspieszenie badań. Kluczową zmianą jest wprowadzenie wymogu, aby szpitale uczestniczące w programie Medicare pytały pacjentów o zgodę na udostępnienie ich danych zdrowotnych do celów badawczych. Ma to zapewnić etyczne wykorzystanie danych oraz rozwój zasobów obliczeniowych i standardów interoperacyjności.\",\n  \"pl_key_points\": [\n    \"Szpitale uczestniczące w programie Medicare będą musiały prosić pacjentów o zgodę na udostępnianie ich danych zdrowotnych do celów badawczych.\",\n    \"Powstają nowe, ujednolicone zasoby danych i standardy interoperacyjności, zarządzane m.in. przez NIH i Krajowego Koordynatora ds. Technologii Informacyjnych w Ochronie Zdrowia.\",\n    \"Autoryzowano łącznie 660 milionów dolarów na rok fiskalny 2025 na finansowanie działań NIH, Krajowego Koordynatora oraz National Library of Medicine.\"\n  ],\n  \"eng_ai_title\": \"Ethical AI Adoption in Healthcare: Data Consent and Research Funding\",\n  \"eng_summary\": \"This bill authorizes funding to accelerate the ethical development of Artificial Intelligence in healthcare, aiming to improve medical treatment and research. Crucially, it establishes a requirement for hospitals participating in Medicare to ask patients for permission before sharing their health data for research purposes. This ensures ethical data use while developing computational resources and interoperability standards.\",\n  \"eng_key_points\": [\n    \"Hospitals participating in Medicare must request patient permission to share health data for health-related research purposes.\",\n    \"The law authorizes a total of $660 million for Fiscal Year 2025 to fund activities by the NIH, the National Coordinator, and the National Library of Medicine.\",\n    \"New federated data resources and interoperability standards will be established to unify access to clinical data for ethical biomedical research.\"\n  ],\n  \"de_ai_title\": \"Ethische KI im Gesundheitswesen: Patientenzustimmung und Forschungsförderung\",\n  \"de_summary\": \"Dieses Gesetz genehmigt Mittel, um die ethische Entwicklung der Künstlichen Intelligenz im Gesundheitswesen zu beschleunigen und die medizinische Versorgung zu verbessern. Eine wichtige Änderung ist die Verpflichtung für Krankenhäuser, die am Medicare-Programm teilnehmen, Patienten um Erlaubnis zu bitten, bevor ihre Gesundheitsdaten für Forschungszwecke weitergegeben werden. Dies soll die ethische Datennutzung sowie die Entwicklung von Rechenressourcen und Interoperabilitätsstandards sicherstellen.\",\n  \"de_key_points\": [\n    \"Krankenhäuser, die am Medicare-Programm teilnehmen, müssen Patienten um Erlaubnis bitten, ihre Gesundheitsdaten für gesundheitsbezogene Forschungszwecke zu teilen.\",\n    \"Es werden insgesamt 660 Millionen Dollar für das Geschäftsjahr 2025 genehmigt, um Aktivitäten des NIH, des National Coordinator und der National Library of Medicine zu finanzieren.\",\n    \"Es werden neue föderierte Datenressourcen und Interoperabilitätsstandards geschaffen, um den Zugang zu klinischen Daten für die ethische biomedizinische Forschung zu vereinheitlichen.\"\n  ],\n  \"fr_ai_title\": \"Adoption éthique de l'IA en santé: consentement des données et financement de la recherche\",\n  \"fr_summary\": \"Ce projet de loi autorise un financement pour accélérer le développement éthique de l'Intelligence Artificielle dans les soins de santé, visant à améliorer le traitement médical. Un changement clé est l'obligation pour les hôpitaux participant à Medicare de demander la permission des patients avant de partager leurs données de santé à des fins de recherche. Cela garantit une utilisation éthique des données tout en développant des ressources informatiques et des normes d'interopérabilité.\",\n  \"fr_key_points\": [\n    \"Les hôpitaux participant à Medicare doivent demander l'autorisation des patients pour partager leurs données de santé à des fins de recherche liée à la santé.\",\n    \"Un total de 660 millions de dollars est autorisé pour l'exercice 2025 afin de financer les activités du NIH, du Coordinateur National et de la National Library of Medicine.\",\n    \"De nouvelles ressources de données fédérées et des normes d'interopérabilité seront établies pour unifier l'accès aux données cliniques pour la recherche biomédicale éthique.\"\n  ],\n  \"es_ai_title\": \"Adopción ética de IA en salud: consentimiento de datos y financiación de investigación\",\n  \"es_summary\": \"Esta legislación autoriza financiación para impulsar el desarrollo ético de la Inteligencia Artificial en la atención médica, con el objetivo de mejorar los tratamientos. Un cambio fundamental es que los hospitales que participan en Medicare deberán solicitar permiso a los pacientes antes de compartir sus datos de salud para fines de investigación. Esto asegura el uso ético de los datos mientras se desarrollan recursos computacionales y estándares de interoperabilidad.\",\n  \"es_key_points\": [\n    \"Los hospitales que participan en Medicare deben solicitar permiso al paciente para compartir sus datos de salud con fines de investigación relacionada con la salud.\",\n    \"Se autoriza un total de 660 millones de dólares para el año fiscal 2025 para financiar actividades del NIH, el Coordinador Nacional y la National Library of Medicine.\",\n    \"Se establecerán nuevos recursos de datos federados y estándares de interoperabilidad para unificar el acceso a la información clínica para la investigación biomédica ética.\"\n  ],\n  \"it_ai_title\": \"Adozione etica dell'IA nella sanità: consenso sui dati e finanziamento della ricerca\",\n  \"it_summary\": \"Questo disegno di legge autorizza finanziamenti per accelerare lo sviluppo etico dell'Intelligenza Artificiale nel settore sanitario, mirando a migliorare i trattamenti medici. Un cambiamento cruciale è l'obbligo per gli ospedali che partecipano a Medicare di chiedere il permesso ai pazienti prima di condividere i loro dati sanitari per scopi di ricerca. Ciò garantisce un uso etico dei dati mentre si sviluppano risorse computazionali e standard di interoperabilità.\",\n  \"it_key_points\": [\n    \"Gli ospedali che partecipano a Medicare devono richiedere il permesso del paziente per condividere i dati sanitari per scopi di ricerca legati alla salute.\",\n    \"Sono autorizzati un totale di 660 milioni di dollari per l'anno fiscale 2025 per finanziare le attività del NIH, del Coordinatore Nazionale e della National Library of Medicine.\",\n    \"Verranno istituite nuove risorse di dati federati e standard di interoperabilità per unificare l'accesso ai dati clinici per la ricerca biomedica etica.\"\n  ],\n  \"nl_ai_title\": \"Ethische AI in de gezondheidszorg: toestemming voor gegevens en onderzoek financiering\",\n  \"nl_summary\": \"Dit wetsvoorstel autoriseert financiering om de ethische ontwikkeling van Kunstmatige Intelligentie in de gezondheidszorg te versnellen, met als doel de medische behandeling te verbeteren. Een cruciale verandering is de verplichting voor ziekenhuizen die deelnemen aan Medicare om patiënten om toestemming te vragen voordat hun gezondheidsgegevens worden gedeeld voor onderzoeksdoeleinden. Dit zorgt voor ethisch gegevensgebruik tijdens de ontwikkeling van computerbronnen en interoperabiliteitsstandaarden.\",\n  \"nl_key_points\": [\n    \"Ziekenhuizen die deelnemen aan Medicare moeten patiënttoestemming vragen om gezondheidsgegevens te delen voor gezondheidsgerelateerde onderzoeksdoeleinden.\",\n    \"Er is in totaal 660 miljoen dollar geautoriseerd voor het fiscale jaar 2025 om activiteiten van de NIH, de Nationale Coördinator en de National Library of Medicine te financieren.\",\n    \"Nieuwe gefedereerde gegevensbronnen en interoperabiliteitsstandaarden zullen worden vastgesteld om de toegang tot klinische gegevens voor ethisch biomedisch onderzoek te verenigen.\"\n  ],\n  \"pt_ai_title\": \"Adoção ética de IA na saúde: consentimento de dados e financiamento de pesquisa\",\n  \"pt_summary\": \"Este projeto de lei autoriza financiamento para acelerar o desenvolvimento ético da Inteligência Artificial nos cuidados de saúde, visando melhorar o tratamento médico. Uma mudança crucial é a obrigação de os hospitais participantes no Medicare solicitarem permissão aos pacientes antes de partilharem os seus dados de saúde para fins de investigação. Isto garante o uso ético de dados enquanto se desenvolvem recursos computacionais e padrões de interoperabilidade.\",\n  \"pt_key_points\": [\n    \"Os hospitais participantes no Medicare devem solicitar a permissão do paciente para partilhar dados de saúde para fins de investigação relacionada com a saúde.\",\n    \"Estão autorizados um total de 660 milhões de dólares para o ano fiscal de 2025 para financiar atividades do NIH, do Coordenador Nacional e da National Library of Medicine.\",\n    \"Novos recursos de dados federados e padrões de interoperabilidade serão estabelecidos para unificar o acesso a dados clínicos para pesquisa biomédica ética.\"\n  ],\n  \"category\": [\n    \"Health\",\n    \"Informatization\"\n  ]\n}"
    },
    {
      "timestamp": "2025-12-30T22:33:48.148Z",
      "source_url": "https://www.congress.gov/118/bills/s4862/BILLS-118s4862is.xml",
      "model": "gemini-flash-lite-latest",
      "prompt_sent": "\nROLE: Fact Checker.\nZADANIE: Porównaj SOURCE (oryginał) i SUMMARY (streszczenie przygotowane przez inne AI).\n\nTwoim celem jest wykrycie \"ZMYŚLONYCH KONKRETÓW\" (Fabricated Entities) w SUMMARY.\n\nSOURCE:\n118 S4862 IS: To ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes. U.S. Senate 2024-07-30 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. II118th CONGRESS2d SessionS. 4862IN THE SENATE OF THE UNITED STATESJuly 30, 2024Mr. Rounds (for himself and Mr. Heinrich) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and PensionsA BILLTo ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes.1.Governing ethical AI use and innovation for health care development(a)National Institutes of HealthPart A of title IV of the Public Health Service Act is amended by inserting after section 403D (42 U.S.C. 283a–3) the following:403E.Artificial intelligence(a)In generalThe Director of NIH shall—(1)develop computational resources and datasets necessary to use artificial intelligence approaches for health and health care research;(2)provide expertise in biomedical research and the use of artificial intelligence;(3)develop and maintain federated resources that provide unified access to data from fundamental biomedical research and the clinical care environment; (4)provide education and ongoing support to a nationwide user community to foster scientifically sound, ethical, and inclusive research using artificial intelligence that addresses the health needs of all individuals; and(5)extend the clinical research capabilities of the National Institutes of Health to address significant gaps in evidence to guide clinical care and to serve the needs of every community.(b)Authorization of appropriationsThere is authorized to be appropriated to the Director of NIH to carry out this section $400,000,000 for fiscal year 2025..(b)Office of the National Coordinator for Health Information TechnologySubtitle C of title XXX of the Public Health Service Act (42 U.S.C. 300jj–51 et seq.) is amended by adding at the end the following:3023.Artificial intelligence(a)In generalThe National Coordinator shall—(1)carry out activities to engage in health research by—(A)utilizing the electronic health record as a data collection tool; and (B)requiring that individuals are offered an opportunity to direct the use of their health data for health care research; and(2)establish data and interoperability standards for access, exchange, and use of clinical and administrative data from the clinical care environment through a National Artificial Intelligence Research Resource, in alignment with—(A)the United States Core Data for Interoperability; (B)the Fast Health Interoperability Resources; and(C)the Trusted Exchange Framework and Common Agreement.(b)Authorization of appropriationsThere are authorized to be appropriated to the National Coordinator for fiscal year 2025—(1)$10,000,000 to carry out subsection (a)(1); and(2)$50,000,000 to carry out subsection (a)(2)..(c)Medicare requirement for hospitals relating to use of electronic health records data for biomedical research purposesSection 1866(a)(1) of the Social Security Act (42 U.S.C. 1395cc(a)(1)) is amended—(1)by moving the indentation of subparagraph (W) 2 ems to the left;(2)in subparagraph (X)—(A)by moving the indentation 2 ems to the left; and(B)by striking and at the end;(3)in subparagraph (Y), by striking the period at the end and inserting ; and; and(4)by inserting after subparagraph (Y) the following new subparagraph:(Z)in the case of a hospital, with respect to each individual who is admitted to the hospital on or after the date that is 1 year after the date of enactment of this subparagraph, to—(i)request permission of the individual to share the health data of the individual for health-related research purposes in accordance with section 3023(a)(1) of the Public Health Service Act; and(ii)in the case where the individual grants permission to the sharing of such data, share the electronic health record of the individual for such purposes in accordance with such section..(d)Sense of the SenateIt is the sense of the Senate that any steering subcommittee (or similar entity) for a National Artificial Intelligence Research Resource established in the Interagency Committee established under section 5103 of the William M. (Mac) Thornberry National Defense Authorization Act for Fiscal Year 2021 (15 U.S.C. 9413) shall include an officer or employee of the National Institutes of Health. (e)National Library of Medicine(1)In generalSection 465(b) of the Public Health Service Act (42 U.S.C. 286(b)) is amended—(A)in paragraph (7), by striking and after the semicolon;(B)by redesignating paragraph (8) as paragraph (10); and(C)by inserting after paragraph (7) the following:(8)establish facilities so that the Library serves as the central exchange center of federated data sharing; (9)establish a core data science program to guide and enable a diverse and comprehensive community of health-related research data users; and.(2)Authorization of appropriationsSubpart 1 of part D of title IV of the Public Health Service Act (42 U.S.C. 286 et seq.) is amended by adding at the end the following:468.Authorization of appropriationsThere are authorized to be appropriated to the Secretary for fiscal year 2025—(1)$100,000,000 to carry out section 465(b)(8); and(2)$100,000,000 to carry out section 465(b)(9)..\n\nSUMMARY TO EVALUATE:\nTitle: Ethical AI Adoption in Healthcare: Data Consent and Research Funding.\nSummary: This bill authorizes significant funding to accelerate the ethical development of Artificial Intelligence in healthcare, aiming to improve medical treatment and research nationwide. Crucially, it establishes new rules requiring hospitals to ask patients for permission before sharing their electronic health records for AI research purposes. This ensures individuals maintain control over how their personal health data is utilized for scientific advancement.\nKey Points: Hospitals participating in Medicare must request patient permission to share Electronic Health Records (EHR) data for health-related research., The law authorizes $660 million for Fiscal Year 2025 to fund federal agencies (NIH, ONC, NLM) to develop AI research resources and data standards., New national data resources and interoperability standards will be established to unify access to clinical data for ethical biomedical AI research.\n\nZASADY OCENY:\n1. Sprawdź wszystkie LICZBY, DATY i KWOTY w SUMMARY. Jeśli którejś brakuje w SOURCE -> is_valid: false.\n2. Sprawdź wszystkie NAZWISKA, ORGANIZACJE i MIEJSCA w SUMMARY. Jeśli którejś brakuje w SOURCE -> is_valid: false.\n3. Sprawdź wszystkie konkretne DZIAŁANIA PRAWNE . Jeśli tego mechanizmu nie ma w SOURCE -> is_valid: false.\n\nWAŻNE: Abstrakcyjne pojęcia (np. \"transparentność\", \"zaufanie\") są dozwolone jako wnioski.\n\nOUTPUT (JSON):\n{\n  \"is_valid\": true/false,\n  \"issue\": \"fabricated_entity\" / \"contradiction\" / \"none\"\n}\n\nWYMAGANIA FORMATOWANIA:\n1. Odpowiedz WYŁĄCZNIE surowym obiektem JSON.\n2. NIE używaj bloków kodu Markdown.\n3. NIE dodawaj żadnych wstępów ani wyjaśnień przed ani po JSONie.\n4. JSON musi być poprawny i gotowy do parsowania.\n\n",
      "ai_response_raw": "{\n  \"is_valid\": false,\n  \"issue\": \"fabricated_entity\"\n}"
    },
    {
      "timestamp": "2025-12-30T16:10:23.263Z",
      "source_url": "https://www.congress.gov/118/bills/s4862/BILLS-118s4862is.xml",
      "model": "gemini-flash-latest",
      "prompt_sent": "\nJesteś ekspertem od prawa Stanów Zjednoczonych, który ma za zadanie analizować dokumenty ustaw, uchwał oraz innych dokumentów legislacyjnych, a następnie przygotowywać z nich informacje w przystępny sposób dla obywateli. Twoim celem jest przedstawienie informacji tak, aby obywatele mogli sami ocenić wpływ legislacji na ich życie, nawet bez posiadania specjalistycznej wiedzy legislacyjnej. Skup się na faktach i konsekwencjach wprowadzanych zmian, unikając wartościowania i osobistych opinii. Wszelki żargon prawny jest zabroniony. Prezentuj informacje w jasny, zwięzły i angażujący sposób, tak aby były zrozumiałe dla osoby bez wykształcenia prawniczego. Unikaj długich, złożonych zdań. Zamiast pisać \"projekt ma na celu nowelizację kodeksu podatkowego...\", napisz \"Zmiany w podatkach: nowe ulgi i obowiązki dla...\". Kontynuuj swoją pracę, dopóki nie rozwiążesz swojego zadania. Jeśli nie masz pewności co do generowanej treści, przeanalizuj dokument ponownie – nie zgaduj. Rozplanuj dobrze swoje zadanie przed przystąpieniem do niego. W podsumowaniu i kluczowych punktach, jeśli to możliwe i uzasadnione, podkreśl, jakie konkretne korzyści lub konsekwencje (pozytywne lub negatywne) wprowadza ustawa dla życia codziennego obywateli, ich praw i obowiązków, finansów osobistych, bezpieczeństwa i innych ważnych kwestii.\n\nTwoja odpowiedź MUSI być w formacie JSON - i zawierać następujące klucze.\nZanim zwrócisz odpowiedź, dokładnie zweryfikuj, czy cała struktura JSON jest w 100% poprawna, włącznie ze wszystkimi przecinkami, nawiasami klamrowymi, kwadratowymi oraz cudzysłowami. Błędny JSON jest nieakceptowalny i uniemożliwi przetworzenie Twojej pracy.\n\nPrzeanalizuj dokładnie poniższy tekst dokumentu prawnego. To jest treść, na podstawie której masz wygenerować podsumowanie i kluczowe punkty:\n--- POCZĄTEK DOKUMENTU ---\n118 S4862 IS: To ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes. U.S. Senate 2024-07-30 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. II118th CONGRESS2d SessionS. 4862IN THE SENATE OF THE UNITED STATESJuly 30, 2024Mr. Rounds (for himself and Mr. Heinrich) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and PensionsA BILLTo ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes.1.Governing ethical AI use and innovation for health care development(a)National Institutes of HealthPart A of title IV of the Public Health Service Act is amended by inserting after section 403D (42 U.S.C. 283a–3) the following:403E.Artificial intelligence(a)In generalThe Director of NIH shall—(1)develop computational resources and datasets necessary to use artificial intelligence approaches for health and health care research;(2)provide expertise in biomedical research and the use of artificial intelligence;(3)develop and maintain federated resources that provide unified access to data from fundamental biomedical research and the clinical care environment; (4)provide education and ongoing support to a nationwide user community to foster scientifically sound, ethical, and inclusive research using artificial intelligence that addresses the health needs of all individuals; and(5)extend the clinical research capabilities of the National Institutes of Health to address significant gaps in evidence to guide clinical care and to serve the needs of every community.(b)Authorization of appropriationsThere is authorized to be appropriated to the Director of NIH to carry out this section $400,000,000 for fiscal year 2025..(b)Office of the National Coordinator for Health Information TechnologySubtitle C of title XXX of the Public Health Service Act (42 U.S.C. 300jj–51 et seq.) is amended by adding at the end the following:3023.Artificial intelligence(a)In generalThe National Coordinator shall—(1)carry out activities to engage in health research by—(A)utilizing the electronic health record as a data collection tool; and (B)requiring that individuals are offered an opportunity to direct the use of their health data for health care research; and(2)establish data and interoperability standards for access, exchange, and use of clinical and administrative data from the clinical care environment through a National Artificial Intelligence Research Resource, in alignment with—(A)the United States Core Data for Interoperability; (B)the Fast Health Interoperability Resources; and(C)the Trusted Exchange Framework and Common Agreement.(b)Authorization of appropriationsThere are authorized to be appropriated to the National Coordinator for fiscal year 2025—(1)$10,000,000 to carry out subsection (a)(1); and(2)$50,000,000 to carry out subsection (a)(2)..(c)Medicare requirement for hospitals relating to use of electronic health records data for biomedical research purposesSection 1866(a)(1) of the Social Security Act (42 U.S.C. 1395cc(a)(1)) is amended—(1)by moving the indentation of subparagraph (W) 2 ems to the left;(2)in subparagraph (X)—(A)by moving the indentation 2 ems to the left; and(B)by striking and at the end;(3)in subparagraph (Y), by striking the period at the end and inserting ; and; and(4)by inserting after subparagraph (Y) the following new subparagraph:(Z)in the case of a hospital, with respect to each individual who is admitted to the hospital on or after the date that is 1 year after the date of enactment of this subparagraph, to—(i)request permission of the individual to share the health data of the individual for health-related research purposes in accordance with section 3023(a)(1) of the Public Health Service Act; and(ii)in the case where the individual grants permission to the sharing of such data, share the electronic health record of the individual for such purposes in accordance with such section..(d)Sense of the SenateIt is the sense of the Senate that any steering subcommittee (or similar entity) for a National Artificial Intelligence Research Resource established in the Interagency Committee established under section 5103 of the William M. (Mac) Thornberry National Defense Authorization Act for Fiscal Year 2021 (15 U.S.C. 9413) shall include an officer or employee of the National Institutes of Health. (e)National Library of Medicine(1)In generalSection 465(b) of the Public Health Service Act (42 U.S.C. 286(b)) is amended—(A)in paragraph (7), by striking and after the semicolon;(B)by redesignating paragraph (8) as paragraph (10); and(C)by inserting after paragraph (7) the following:(8)establish facilities so that the Library serves as the central exchange center of federated data sharing; (9)establish a core data science program to guide and enable a diverse and comprehensive community of health-related research data users; and.(2)Authorization of appropriationsSubpart 1 of part D of title IV of the Public Health Service Act (42 U.S.C. 286 et seq.) is amended by adding at the end the following:468.Authorization of appropriationsThere are authorized to be appropriated to the Secretary for fiscal year 2025—(1)$100,000,000 to carry out section 465(b)(8); and(2)$100,000,000 to carry out section 465(b)(9)..\n--- KONIEC DOKUMENTU ---\n\nPAMIĘTAJ: Twoja odpowiedź MUSI być wyłącznie poprawnym obiektem JSON. Nie dodawaj żadnych dodatkowych znaków, komentarzy ani tekstu przed znacznikiem '{' ani po znaczniku '}'. Cała odpowiedź musi być parsowalna jako JSON.\nNa podstawie POWYŻSZEGO dokumentu, wypełnij poniższą strukturę JSON:\nOto struktura JSON, której oczekuję (wypełnij ją treścią):\n{\n  \"pl_ai_title\": \"Nowy, krótki tytuł dla aktu prawnego po polsku, oddający sedno wprowadzanych zmian (np. maksymalnie 10-12 słów).\",\n  \"pl_summary\": \"2-3 zdania zwięzłego podsumowania treści aktu prawnego po polsku, napisane z perspektywy wpływu na życie codzienne obywateli.\",\n  \"pl_key_points\": [\n    \"Pierwszy krótki punkt po polsku dotyczący najważniejszych wprowadzanych rozwiązań lub zmian.\",\n    \"Drugi krótki punkt po polsku...\"\n  ],\n  \"eng_ai_title\": \"A new, short title for the legal act in English, capturing the essence of the changes (e.g., max 10-12 words).\",\n  \"eng_summary\": \"2-3 sentences summarizing the legal act in English, from the perspective of its impact on citizens' daily lives.\",\n  \"eng_key_points\": [\n    \"First short bullet point in English regarding the most important solutions or changes being introduced.\",\n    \"Second short bullet point in English...\"\n  ],\n  \"de_ai_title\": \"Ein neuer, kurzer Titel für das Rechtsdokument auf Deutsch, der den Kern der Änderungen erfasst (z.B. max. 10-12 Wörter).\",\n  \"de_summary\": \"2-3 Sätze Zusammenfassung des Rechtsdokuments auf Deutsch, aus der Perspektive seiner Auswirkungen auf das tägliche Leben der Bürger.\",\n  \"de_key_points\": [\n    \"Erster kurzer Stichpunkt auf Deutsch zu den wichtigsten eingeführten Lösungen oder Änderungen.\",\n    \"Zweiter kurzer Stichpunkt auf Deutsch...\"\n  ],\n  \"fr_ai_title\": \"Un nouveau titre court pour l'acte juridique en français, saisissant l'essence des changements (par exemple, 10-12 mots maximum).\",\n  \"fr_summary\": \"Résumé de 2-3 phrases de l'acte juridique en français, du point de vue de son impact sur la vie quotidienne des citoyens.\",\n  \"fr_key_points\": [\n    \"Premier court point en français concernant les solutions ou changements les plus importants introduits.\",\n    \"Deuxième court point en français...\"\n  ],\n  \"es_ai_title\": \"Un nuevo título breve para el acto jurídico en español, que recoja la esencia de los cambios (por ejemplo, máximo 10-12 palabras).\",\n  \"es_summary\": \"Resumen de 2-3 frases del acto jurídico en español, desde la perspectiva de su impacto en la vida cotidiana de los ciudadanos.\",\n  \"es_key_points\": [\n    \"Primer punto breve en español sobre las soluciones o cambios más importantes que se introducen.\",\n    \"Segundo punto breve en español...\"\n  ],\n  \"it_ai_title\": \"Un nuovo titolo breve per l'atto giuridico in italiano, che colga l'essenza delle modifiche (ad es. massimo 10-12 parole).\",\n  \"it_summary\": \"Riepilogo di 2-3 frasi dell'atto giuridico in italiano, dal punto di vista del suo impatto sulla vita quotidiana dei cittadini.\",\n  \"it_key_points\": [\n    \"Primo breve punto in italiano riguardante le soluzioni o le modifiche più importanti introdotte.\",\n    \"Secondo breve punto in italiano...\"\n  ],\n  \"nl_ai_title\": \"Een nieuwe, korte titel voor de rechtshandeling in het Nederlands, die de essentie van de wijzigingen weergeeft (bijv. max. 10-12 woorden).\",\n  \"nl_summary\": \"Samenvatting van 2-3 zinnen van de rechtshandeling in het Nederlands, vanuit het perspectief van de impact op het dagelijks leven van burgers.\",\n  \"nl_key_points\": [\n    \"Eerste korte punt in het Nederlands betreffende de belangrijkste geïntroduceerde oplossingen of wijzigingen.\",\n    \"Tweede korte punt in het Nederlands...\"\n  ],\n  \"pt_ai_title\": \"Um novo título curto para o ato jurídico em português, capturando a essência das mudanças (por exemplo, máx. 10-12 palavras).\",\n  \"pt_summary\": \"Resumo de 2-3 frases do ato jurídico em português, na perspetiva do seu impacto na vida quotidiana dos cidadãos.\",\n  \"pt_key_points\": [\n    \"Primeiro ponto curto em português sobre as soluções ou alterações mais importantes introduzidas.\",\n    \"Segundo ponto curto em português...\"\n  ],\n  \"category\": [\"Categorize the document into one category by default, based on the field it primarily concerns. Choose up to 3 if the document also touches upon SIGNIFICANT issues from other categories. You MUST select categories ONLY from the following list: Health, Education, Family, Taxes, Labor, Security, Environment, Courts and Law, Transport, Benefits, Real Estate, Media and Culture, Local Government, Migration, Agriculture, Public Investments, Informatization, Economy. If the document does not definitively fit any of these, you MUST use \"Other\". If you use \"Other\", it should be the ONLY category selected. Do NOT invent new categories. The response must be an array of strings, e.g., [\"Taxes\", \"Family\"].\"]\n}\n\n",
      "ai_response_raw": "{\n  \"pl_ai_title\": \"Etyczne wykorzystanie sztucznej inteligencji w badaniach medycznych i opiece zdrowotnej.\",\n  \"pl_summary\": \"Ustawa przeznacza setki milionów dolarów na rozwój sztucznej inteligencji w służbie zdrowia, mając na celu poprawę opieki medycznej i przyspieszenie badań. Kluczową zmianą dla obywateli jest wprowadzenie obowiązku pytania pacjentów przez szpitale o zgodę na wykorzystanie ich elektronicznej dokumentacji medycznej w celach badawczych. Ma to zapewnić etyczne i kontrolowane wykorzystanie danych do tworzenia nowych narzędzi diagnostycznych i leczniczych.\",\n  \"pl_key_points\": [\n    \"Szpitale uczestniczące w programie Medicare będą musiały prosić pacjentów o zgodę na udostępnianie ich elektronicznej dokumentacji medycznej (EHR) do celów badawczych.\",\n    \"Powstają nowe, ujednolicone zasoby danych na poziomie krajowym, zarządzane przez NIH i ONC, aby przyspieszyć rozwój etycznej sztucznej inteligencji w medycynie.\",\n    \"Autoryzowano przeznaczenie 660 milionów dolarów na rok fiskalny 2025 na finansowanie tych działań, w tym na tworzenie zasobów obliczeniowych i edukację w zakresie AI.\"\n  ],\n  \"eng_ai_title\": \"Ethical AI Adoption in Healthcare: Data Consent and Research Funding.\",\n  \"eng_summary\": \"This bill authorizes significant funding to accelerate the ethical development of Artificial Intelligence in healthcare, aiming to improve medical treatment and research nationwide. Crucially, it establishes new rules requiring hospitals to ask patients for permission before sharing their electronic health records for AI research purposes. This ensures individuals maintain control over how their personal health data is utilized for scientific advancement.\",\n  \"eng_key_points\": [\n    \"Hospitals participating in Medicare must request patient permission to share Electronic Health Records (EHR) data for health-related research.\",\n    \"The law authorizes $660 million for Fiscal Year 2025 to fund federal agencies (NIH, ONC, NLM) to develop AI research resources and data standards.\",\n    \"New national data resources and interoperability standards will be established to unify access to clinical data for ethical biomedical AI research.\"\n  ],\n  \"de_ai_title\": \"Ethische KI im Gesundheitswesen: Patientenzustimmung und Forschungsförderung.\",\n  \"de_summary\": \"Dieses Gesetz genehmigt erhebliche Mittel, um die ethische Entwicklung der Künstlichen Intelligenz im Gesundheitswesen zu beschleunigen und die medizinische Versorgung zu verbessern. Eine wichtige Änderung ist die Verpflichtung für Krankenhäuser, Patienten um Erlaubnis zu bitten, bevor ihre elektronischen Gesundheitsdaten für KI-Forschungszwecke weitergegeben werden. Dies stärkt die Kontrolle der Bürger über ihre persönlichen Gesundheitsdaten.\",\n  \"de_key_points\": [\n    \"Krankenhäuser, die am Medicare-Programm teilnehmen, müssen Patienten um Erlaubnis bitten, ihre elektronischen Gesundheitsakten (EHR) für Forschungszwecke zu teilen.\",\n    \"Es werden 660 Millionen Dollar für das Geschäftsjahr 2025 bereitgestellt, um Bundesbehörden (NIH, ONC) bei der Entwicklung von KI-Forschungsressourcen und Datenstandards zu unterstützen.\",\n    \"Es werden neue nationale Datenressourcen und Interoperabilitätsstandards geschaffen, um den Zugang zu klinischen Daten für ethische biomedizinische KI-Forschung zu vereinheitlichen.\"\n  ],\n  \"fr_ai_title\": \"Adoption éthique de l'IA en santé: consentement des données et financement de la recherche.\",\n  \"fr_summary\": \"Ce projet de loi autorise un financement important pour accélérer le développement éthique de l'Intelligence Artificielle dans les soins de santé, visant à améliorer le traitement médical. Un changement clé pour les citoyens est l'obligation pour les hôpitaux de demander la permission des patients avant de partager leurs dossiers de santé électroniques à des fins de recherche en IA. Cela garantit que les individus gardent le contrôle sur l'utilisation de leurs données de santé personnelles.\",\n  \"fr_key_points\": [\n    \"Les hôpitaux participant à Medicare doivent demander l'autorisation des patients pour partager leurs dossiers de santé électroniques (DSE) à des fins de recherche.\",\n    \"660 millions de dollars sont autorisés pour l'exercice 2025 afin de financer les agences fédérales (NIH, ONC) pour développer des ressources de recherche en IA et des normes de données.\",\n    \"De nouvelles ressources nationales de données et des normes d'interopérabilité seront établies pour unifier l'accès aux données cliniques pour la recherche biomédicale éthique.\"\n  ],\n  \"es_ai_title\": \"Adopción ética de IA en salud: consentimiento de datos y financiación de investigación.\",\n  \"es_summary\": \"Esta legislación autoriza una financiación sustancial para impulsar el desarrollo ético de la Inteligencia Artificial en la atención médica, con el objetivo de mejorar los tratamientos. Un cambio fundamental para los ciudadanos es que los hospitales deberán solicitar permiso a los pacientes antes de compartir sus registros de salud electrónicos para la investigación con IA. Esto asegura que las personas mantengan el control sobre cómo se utilizan sus datos personales de salud.\",\n  \"es_key_points\": [\n    \"Los hospitales que participan en Medicare deben solicitar permiso al paciente para compartir los datos de sus Registros de Salud Electrónicos (RSE) con fines de investigación.\",\n    \"Se autorizan 660 millones de dólares para el año fiscal 2025 para financiar agencias federales (NIH, ONC) en el desarrollo de recursos de investigación de IA y estándares de datos.\",\n    \"Se establecerán nuevos recursos nacionales de datos y estándares de interoperabilidad para unificar el acceso a la información clínica para la investigación biomédica ética.\"\n  ],\n  \"it_ai_title\": \"Adozione etica dell'IA nella sanità: consenso sui dati e finanziamento della ricerca.\",\n  \"it_summary\": \"Questo disegno di legge autorizza finanziamenti significativi per accelerare lo sviluppo etico dell'Intelligenza Artificiale nel settore sanitario, mirando a migliorare i trattamenti medici. Un cambiamento cruciale per i cittadini è l'obbligo per gli ospedali di chiedere il permesso ai pazienti prima di condividere le loro cartelle cliniche elettroniche per scopi di ricerca sull'IA. Ciò garantisce che gli individui mantengano il controllo sull'utilizzo dei propri dati sanitari personali.\",\n  \"it_key_points\": [\n    \"Gli ospedali che partecipano a Medicare devono richiedere il permesso del paziente per condividere i dati delle cartelle cliniche elettroniche (EHR) per scopi di ricerca sanitaria.\",\n    \"Sono autorizzati 660 milioni di dollari per l'anno fiscale 2025 per finanziare le agenzie federali (NIH, ONC) nello sviluppo di risorse di ricerca sull'IA e standard di dati.\",\n    \"Verranno istituite nuove risorse nazionali di dati e standard di interoperabilità per unificare l'accesso ai dati clinici per la ricerca biomedica etica.\"\n  ],\n  \"nl_ai_title\": \"Ethische AI in de gezondheidszorg: toestemming voor gegevens en onderzoek financiering.\",\n  \"nl_summary\": \"Dit wetsvoorstel autoriseert aanzienlijke financiering om de ethische ontwikkeling van Kunstmatige Intelligentie in de gezondheidszorg te versnellen, met als doel de medische behandeling te verbeteren. Een cruciale verandering voor burgers is de verplichting voor ziekenhuizen om patiënten om toestemming te vragen voordat hun elektronische medische dossiers worden gedeeld voor AI-onderzoek. Dit zorgt ervoor dat individuen controle behouden over hoe hun persoonlijke gezondheidsgegevens worden gebruikt.\",\n  \"nl_key_points\": [\n    \"Ziekenhuizen die deelnemen aan Medicare moeten patiënttoestemming vragen om Elektronische Gezondheidsdossiers (EGD) te delen voor gezondheidsgerelateerde onderzoeksdoeleinden.\",\n    \"Er is 660 miljoen dollar geautoriseerd voor het fiscale jaar 2025 om federale instanties (NIH, ONC) te financieren voor de ontwikkeling van AI-onderzoeksbronnen en datastandaarden.\",\n    \"Nieuwe nationale gegevensbronnen en interoperabiliteitsstandaarden zullen worden vastgesteld om de toegang tot klinische gegevens voor ethisch biomedisch AI-onderzoek te verenigen.\"\n  ],\n  \"pt_ai_title\": \"Adoção ética de IA na saúde: consentimento de dados e financiamento de pesquisa.\",\n  \"pt_summary\": \"Este projeto de lei autoriza financiamento significativo para acelerar o desenvolvimento ético da Inteligência Artificial nos cuidados de saúde, visando melhorar o tratamento médico. Uma mudança crucial para os cidadãos é a obrigação de os hospitais solicitarem permissão aos pacientes antes de partilharem os seus registos de saúde eletrónicos para fins de pesquisa de IA. Isto garante que os indivíduos mantêm o controlo sobre a utilização dos seus dados pessoais de saúde.\",\n  \"pt_key_points\": [\n    \"Os hospitais participantes no Medicare devem solicitar a permissão do paciente para partilhar dados de Registos Eletrónicos de Saúde (RES) para fins de investigação.\",\n    \"Estão autorizados 660 milhões de dólares para o ano fiscal de 2025 para financiar agências federais (NIH, ONC) no desenvolvimento de recursos de pesquisa de IA e padrões de dados.\",\n    \"Novos recursos nacionais de dados e padrões de interoperabilidade serão estabelecidos para unificar o acesso a dados clínicos para pesquisa biomédica ética.\"\n  ],\n  \"category\": [\n    \"Health\",\n    \"Informatization\"\n  ]\n}"
    },
    {
      "timestamp": "2025-12-26T21:17:18.215Z",
      "source_url": "https://www.congress.gov/118/bills/s4862/BILLS-118s4862is.xml",
      "model": "gemini-flash-lite-latest",
      "prompt_sent": "\nROLE: Fact Checker.\nZADANIE: Porównaj SOURCE (oryginał) i SUMMARY (streszczenie przygotowane przez inne AI).\n\nTwoim celem jest wykrycie \"ZMYŚLONYCH KONKRETÓW\" (Fabricated Entities) w SUMMARY.\n\nSOURCE:\n118 S4862 IS: To ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes. U.S. Senate 2024-07-30 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. II118th CONGRESS2d SessionS. 4862IN THE SENATE OF THE UNITED STATESJuly 30, 2024Mr. Rounds (for himself and Mr. Heinrich) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and PensionsA BILLTo ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes.1.Governing ethical AI use and innovation for health care development(a)National Institutes of HealthPart A of title IV of the Public Health Service Act is amended by inserting after section 403D (42 U.S.C. 283a–3) the following:403E.Artificial intelligence(a)In generalThe Director of NIH shall—(1)develop computational resources and datasets necessary to use artificial intelligence approaches for health and health care research;(2)provide expertise in biomedical research and the use of artificial intelligence;(3)develop and maintain federated resources that provide unified access to data from fundamental biomedical research and the clinical care environment; (4)provide education and ongoing support to a nationwide user community to foster scientifically sound, ethical, and inclusive research using artificial intelligence that addresses the health needs of all individuals; and(5)extend the clinical research capabilities of the National Institutes of Health to address significant gaps in evidence to guide clinical care and to serve the needs of every community.(b)Authorization of appropriationsThere is authorized to be appropriated to the Director of NIH to carry out this section $400,000,000 for fiscal year 2025..(b)Office of the National Coordinator for Health Information TechnologySubtitle C of title XXX of the Public Health Service Act (42 U.S.C. 300jj–51 et seq.) is amended by adding at the end the following:3023.Artificial intelligence(a)In generalThe National Coordinator shall—(1)carry out activities to engage in health research by—(A)utilizing the electronic health record as a data collection tool; and (B)requiring that individuals are offered an opportunity to direct the use of their health data for health care research; and(2)establish data and interoperability standards for access, exchange, and use of clinical and administrative data from the clinical care environment through a National Artificial Intelligence Research Resource, in alignment with—(A)the United States Core Data for Interoperability; (B)the Fast Health Interoperability Resources; and(C)the Trusted Exchange Framework and Common Agreement.(b)Authorization of appropriationsThere are authorized to be appropriated to the National Coordinator for fiscal year 2025—(1)$10,000,000 to carry out subsection (a)(1); and(2)$50,000,000 to carry out subsection (a)(2)..(c)Medicare requirement for hospitals relating to use of electronic health records data for biomedical research purposesSection 1866(a)(1) of the Social Security Act (42 U.S.C. 1395cc(a)(1)) is amended—(1)by moving the indentation of subparagraph (W) 2 ems to the left;(2)in subparagraph (X)—(A)by moving the indentation 2 ems to the left; and(B)by striking and at the end;(3)in subparagraph (Y), by striking the period at the end and inserting ; and; and(4)by inserting after subparagraph (Y) the following new subparagraph:(Z)in the case of a hospital, with respect to each individual who is admitted to the hospital on or after the date that is 1 year after the date of enactment of this subparagraph, to—(i)request permission of the individual to share the health data of the individual for health-related research purposes in accordance with section 3023(a)(1) of the Public Health Service Act; and(ii)in the case where the individual grants permission to the sharing of such data, share the electronic health record of the individual for such purposes in accordance with such section..(d)Sense of the SenateIt is the sense of the Senate that any steering subcommittee (or similar entity) for a National Artificial Intelligence Research Resource established in the Interagency Committee established under section 5103 of the William M. (Mac) Thornberry National Defense Authorization Act for Fiscal Year 2021 (15 U.S.C. 9413) shall include an officer or employee of the National Institutes of Health. (e)National Library of Medicine(1)In generalSection 465(b) of the Public Health Service Act (42 U.S.C. 286(b)) is amended—(A)in paragraph (7), by striking and after the semicolon;(B)by redesignating paragraph (8) as paragraph (10); and(C)by inserting after paragraph (7) the following:(8)establish facilities so that the Library serves as the central exchange center of federated data sharing; (9)establish a core data science program to guide and enable a diverse and comprehensive community of health-related research data users; and.(2)Authorization of appropriationsSubpart 1 of part D of title IV of the Public Health Service Act (42 U.S.C. 286 et seq.) is amended by adding at the end the following:468.Authorization of appropriationsThere are authorized to be appropriated to the Secretary for fiscal year 2025—(1)$100,000,000 to carry out section 465(b)(8); and(2)$100,000,000 to carry out section 465(b)(9)..\n\nSUMMARY TO EVALUATE:\nTitle: Ethical AI Adoption in Healthcare: Data Consent and Research Funding.\nSummary: This bill authorizes significant funding to accelerate the ethical development of Artificial Intelligence in healthcare, aiming to improve medical treatment and research nationwide. Crucially, it establishes new rules requiring hospitals to ask patients for permission before sharing their electronic health records for AI research purposes. This ensures individuals maintain control over how their personal health data is utilized for scientific advancement.\nKey Points: Hospitals participating in Medicare must request patient permission to share Electronic Health Records (EHR) data for health-related research., The law authorizes $660 million for Fiscal Year 2025 to fund federal agencies (NIH, ONC, NLM) to develop AI research resources and data standards., New national data resources and interoperability standards will be established to unify access to clinical data for ethical biomedical AI research.\n\nZASADY OCENY:\n1. Sprawdź wszystkie LICZBY, DATY i KWOTY w SUMMARY. Jeśli którejś brakuje w SOURCE -> is_valid: false.\n2. Sprawdź wszystkie NAZWISKA, ORGANIZACJE i MIEJSCA w SUMMARY. Jeśli którejś brakuje w SOURCE -> is_valid: false.\n3. Sprawdź wszystkie konkretne DZIAŁANIA PRAWNE . Jeśli tego mechanizmu nie ma w SOURCE -> is_valid: false.\n\nWAŻNE: Abstrakcyjne pojęcia (np. \"transparentność\", \"zaufanie\") są dozwolone jako wnioski.\n\nOUTPUT (JSON):\n{\n  \"is_valid\": true/false,\n  \"issue\": \"fabricated_entity\" / \"contradiction\" / \"none\"\n}\n\nWYMAGANIA FORMATOWANIA:\n1. Odpowiedz WYŁĄCZNIE surowym obiektem JSON.\n2. NIE używaj bloków kodu Markdown.\n3. NIE dodawaj żadnych wstępów ani wyjaśnień przed ani po JSONie.\n4. JSON musi być poprawny i gotowy do parsowania.\n\n",
      "ai_response_raw": "{\n  \"is_valid\": false,\n  \"issue\": \"fabricated_entity\"\n}"
    },
    {
      "timestamp": "2025-12-23T06:38:42.039Z",
      "source_url": "https://www.congress.gov/118/bills/s4862/BILLS-118s4862is.xml",
      "model": "gemini-flash-latest",
      "prompt_sent": "\nJesteś ekspertem od prawa Stanów Zjednoczonych, który ma za zadanie analizować dokumenty ustaw, uchwał oraz innych dokumentów legislacyjnych, a następnie przygotowywać z nich informacje w przystępny sposób dla obywateli. Twoim celem jest przedstawienie informacji tak, aby obywatele mogli sami ocenić wpływ legislacji na ich życie, nawet bez posiadania specjalistycznej wiedzy legislacyjnej. Skup się na faktach i konsekwencjach wprowadzanych zmian, unikając wartościowania i osobistych opinii. Wszelki żargon prawny jest zabroniony. Prezentuj informacje w jasny, zwięzły i angażujący sposób, tak aby były zrozumiałe dla osoby bez wykształcenia prawniczego. Unikaj długich, złożonych zdań. Zamiast pisać \"projekt ma na celu nowelizację kodeksu podatkowego...\", napisz \"Zmiany w podatkach: nowe ulgi i obowiązki dla...\". Kontynuuj swoją pracę, dopóki nie rozwiążesz swojego zadania. Jeśli nie masz pewności co do generowanej treści, przeanalizuj dokument ponownie – nie zgaduj. Rozplanuj dobrze swoje zadanie przed przystąpieniem do niego. W podsumowaniu i kluczowych punktach, jeśli to możliwe i uzasadnione, podkreśl, jakie konkretne korzyści lub konsekwencje (pozytywne lub negatywne) wprowadza ustawa dla życia codziennego obywateli, ich praw i obowiązków, finansów osobistych, bezpieczeństwa i innych ważnych kwestii.\n\nTwoja odpowiedź MUSI być w formacie JSON - i zawierać następujące klucze.\nZanim zwrócisz odpowiedź, dokładnie zweryfikuj, czy cała struktura JSON jest w 100% poprawna, włącznie ze wszystkimi przecinkami, nawiasami klamrowymi, kwadratowymi oraz cudzysłowami. Błędny JSON jest nieakceptowalny i uniemożliwi przetworzenie Twojej pracy.\n\nPrzeanalizuj dokładnie poniższy tekst dokumentu prawnego. To jest treść, na podstawie której masz wygenerować podsumowanie i kluczowe punkty:\n--- POCZĄTEK DOKUMENTU ---\n118 S4862 IS: To ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes. U.S. Senate 2024-07-30 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. II118th CONGRESS2d SessionS. 4862IN THE SENATE OF THE UNITED STATESJuly 30, 2024Mr. Rounds (for himself and Mr. Heinrich) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and PensionsA BILLTo ensure that new advances in artificial intelligence are ethically adopted to improve the health of all individuals, and for other purposes.1.Governing ethical AI use and innovation for health care development(a)National Institutes of HealthPart A of title IV of the Public Health Service Act is amended by inserting after section 403D (42 U.S.C. 283a–3) the following:403E.Artificial intelligence(a)In generalThe Director of NIH shall—(1)develop computational resources and datasets necessary to use artificial intelligence approaches for health and health care research;(2)provide expertise in biomedical research and the use of artificial intelligence;(3)develop and maintain federated resources that provide unified access to data from fundamental biomedical research and the clinical care environment; (4)provide education and ongoing support to a nationwide user community to foster scientifically sound, ethical, and inclusive research using artificial intelligence that addresses the health needs of all individuals; and(5)extend the clinical research capabilities of the National Institutes of Health to address significant gaps in evidence to guide clinical care and to serve the needs of every community.(b)Authorization of appropriationsThere is authorized to be appropriated to the Director of NIH to carry out this section $400,000,000 for fiscal year 2025..(b)Office of the National Coordinator for Health Information TechnologySubtitle C of title XXX of the Public Health Service Act (42 U.S.C. 300jj–51 et seq.) is amended by adding at the end the following:3023.Artificial intelligence(a)In generalThe National Coordinator shall—(1)carry out activities to engage in health research by—(A)utilizing the electronic health record as a data collection tool; and (B)requiring that individuals are offered an opportunity to direct the use of their health data for health care research; and(2)establish data and interoperability standards for access, exchange, and use of clinical and administrative data from the clinical care environment through a National Artificial Intelligence Research Resource, in alignment with—(A)the United States Core Data for Interoperability; (B)the Fast Health Interoperability Resources; and(C)the Trusted Exchange Framework and Common Agreement.(b)Authorization of appropriationsThere are authorized to be appropriated to the National Coordinator for fiscal year 2025—(1)$10,000,000 to carry out subsection (a)(1); and(2)$50,000,000 to carry out subsection (a)(2)..(c)Medicare requirement for hospitals relating to use of electronic health records data for biomedical research purposesSection 1866(a)(1) of the Social Security Act (42 U.S.C. 1395cc(a)(1)) is amended—(1)by moving the indentation of subparagraph (W) 2 ems to the left;(2)in subparagraph (X)—(A)by moving the indentation 2 ems to the left; and(B)by striking and at the end;(3)in subparagraph (Y), by striking the period at the end and inserting ; and; and(4)by inserting after subparagraph (Y) the following new subparagraph:(Z)in the case of a hospital, with respect to each individual who is admitted to the hospital on or after the date that is 1 year after the date of enactment of this subparagraph, to—(i)request permission of the individual to share the health data of the individual for health-related research purposes in accordance with section 3023(a)(1) of the Public Health Service Act; and(ii)in the case where the individual grants permission to the sharing of such data, share the electronic health record of the individual for such purposes in accordance with such section..(d)Sense of the SenateIt is the sense of the Senate that any steering subcommittee (or similar entity) for a National Artificial Intelligence Research Resource established in the Interagency Committee established under section 5103 of the William M. (Mac) Thornberry National Defense Authorization Act for Fiscal Year 2021 (15 U.S.C. 9413) shall include an officer or employee of the National Institutes of Health. (e)National Library of Medicine(1)In generalSection 465(b) of the Public Health Service Act (42 U.S.C. 286(b)) is amended—(A)in paragraph (7), by striking and after the semicolon;(B)by redesignating paragraph (8) as paragraph (10); and(C)by inserting after paragraph (7) the following:(8)establish facilities so that the Library serves as the central exchange center of federated data sharing; (9)establish a core data science program to guide and enable a diverse and comprehensive community of health-related research data users; and.(2)Authorization of appropriationsSubpart 1 of part D of title IV of the Public Health Service Act (42 U.S.C. 286 et seq.) is amended by adding at the end the following:468.Authorization of appropriationsThere are authorized to be appropriated to the Secretary for fiscal year 2025—(1)$100,000,000 to carry out section 465(b)(8); and(2)$100,000,000 to carry out section 465(b)(9)..\n--- KONIEC DOKUMENTU ---\n\nPAMIĘTAJ: Twoja odpowiedź MUSI być wyłącznie poprawnym obiektem JSON. Nie dodawaj żadnych dodatkowych znaków, komentarzy ani tekstu przed znacznikiem '{' ani po znaczniku '}'. Cała odpowiedź musi być parsowalna jako JSON.\nNa podstawie POWYŻSZEGO dokumentu, wypełnij poniższą strukturę JSON:\nOto struktura JSON, której oczekuję (wypełnij ją treścią):\n{\n  \"pl_ai_title\": \"Nowy, krótki tytuł dla aktu prawnego po polsku, oddający sedno wprowadzanych zmian (np. maksymalnie 10-12 słów).\",\n  \"pl_summary\": \"2-3 zdania zwięzłego podsumowania treści aktu prawnego po polsku, napisane z perspektywy wpływu na życie codzienne obywateli.\",\n  \"pl_key_points\": [\n    \"Pierwszy krótki punkt po polsku dotyczący najważniejszych wprowadzanych rozwiązań lub zmian.\",\n    \"Drugi krótki punkt po polsku...\"\n  ],\n  \"eng_ai_title\": \"A new, short title for the legal act in English, capturing the essence of the changes (e.g., max 10-12 words).\",\n  \"eng_summary\": \"2-3 sentences summarizing the legal act in English, from the perspective of its impact on citizens' daily lives.\",\n  \"eng_key_points\": [\n    \"First short bullet point in English regarding the most important solutions or changes being introduced.\",\n    \"Second short bullet point in English...\"\n  ],\n  \"de_ai_title\": \"Ein neuer, kurzer Titel für das Rechtsdokument auf Deutsch, der den Kern der Änderungen erfasst (z.B. max. 10-12 Wörter).\",\n  \"de_summary\": \"2-3 Sätze Zusammenfassung des Rechtsdokuments auf Deutsch, aus der Perspektive seiner Auswirkungen auf das tägliche Leben der Bürger.\",\n  \"de_key_points\": [\n    \"Erster kurzer Stichpunkt auf Deutsch zu den wichtigsten eingeführten Lösungen oder Änderungen.\",\n    \"Zweiter kurzer Stichpunkt auf Deutsch...\"\n  ],\n  \"fr_ai_title\": \"Un nouveau titre court pour l'acte juridique en français, saisissant l'essence des changements (par exemple, 10-12 mots maximum).\",\n  \"fr_summary\": \"Résumé de 2-3 phrases de l'acte juridique en français, du point de vue de son impact sur la vie quotidienne des citoyens.\",\n  \"fr_key_points\": [\n    \"Premier court point en français concernant les solutions ou changements les plus importants introduits.\",\n    \"Deuxième court point en français...\"\n  ],\n  \"es_ai_title\": \"Un nuevo título breve para el acto jurídico en español, que recoja la esencia de los cambios (por ejemplo, máximo 10-12 palabras).\",\n  \"es_summary\": \"Resumen de 2-3 frases del acto jurídico en español, desde la perspectiva de su impacto en la vida cotidiana de los ciudadanos.\",\n  \"es_key_points\": [\n    \"Primer punto breve en español sobre las soluciones o cambios más importantes que se introducen.\",\n    \"Segundo punto breve en español...\"\n  ],\n  \"it_ai_title\": \"Un nuovo titolo breve per l'atto giuridico in italiano, che colga l'essenza delle modifiche (ad es. massimo 10-12 parole).\",\n  \"it_summary\": \"Riepilogo di 2-3 frasi dell'atto giuridico in italiano, dal punto di vista del suo impatto sulla vita quotidiana dei cittadini.\",\n  \"it_key_points\": [\n    \"Primo breve punto in italiano riguardante le soluzioni o le modifiche più importanti introdotte.\",\n    \"Secondo breve punto in italiano...\"\n  ],\n  \"nl_ai_title\": \"Een nieuwe, korte titel voor de rechtshandeling in het Nederlands, die de essentie van de wijzigingen weergeeft (bijv. max. 10-12 woorden).\",\n  \"nl_summary\": \"Samenvatting van 2-3 zinnen van de rechtshandeling in het Nederlands, vanuit het perspectief van de impact op het dagelijks leven van burgers.\",\n  \"nl_key_points\": [\n    \"Eerste korte punt in het Nederlands betreffende de belangrijkste geïntroduceerde oplossingen of wijzigingen.\",\n    \"Tweede korte punt in het Nederlands...\"\n  ],\n  \"pt_ai_title\": \"Um novo título curto para o ato jurídico em português, capturando a essência das mudanças (por exemplo, máx. 10-12 palavras).\",\n  \"pt_summary\": \"Resumo de 2-3 frases do ato jurídico em português, na perspetiva do seu impacto na vida quotidiana dos cidadãos.\",\n  \"pt_key_points\": [\n    \"Primeiro ponto curto em português sobre as soluções ou alterações mais importantes introduzidas.\",\n    \"Segundo ponto curto em português...\"\n  ],\n  \"category\": [\"Categorize the document into one category by default, based on the field it primarily concerns. Choose up to 3 if the document also touches upon SIGNIFICANT issues from other categories. You MUST select categories ONLY from the following list: Health, Education, Family, Taxes, Labor, Security, Environment, Courts and Law, Transport, Benefits, Real Estate, Media and Culture, Local Government, Migration, Agriculture, Public Investments, Informatization, Economy. If the document does not definitively fit any of these, you MUST use \"Other\". If you use \"Other\", it should be the ONLY category selected. Do NOT invent new categories. The response must be an array of strings, e.g., [\"Taxes\", \"Family\"].\"]\n}\n\n",
      "ai_response_raw": "{\n  \"pl_ai_title\": \"Etyczne wykorzystanie sztucznej inteligencji w badaniach medycznych i opiece zdrowotnej.\",\n  \"pl_summary\": \"Ustawa przeznacza setki milionów dolarów na rozwój sztucznej inteligencji w służbie zdrowia, mając na celu poprawę opieki medycznej i przyspieszenie badań. Kluczową zmianą dla obywateli jest wprowadzenie obowiązku pytania pacjentów przez szpitale o zgodę na wykorzystanie ich elektronicznej dokumentacji medycznej w celach badawczych. Ma to zapewnić etyczne i kontrolowane wykorzystanie danych do tworzenia nowych narzędzi diagnostycznych i leczniczych.\",\n  \"pl_key_points\": [\n    \"Szpitale uczestniczące w programie Medicare będą musiały prosić pacjentów o zgodę na udostępnianie ich elektronicznej dokumentacji medycznej (EHR) do celów badawczych.\",\n    \"Powstają nowe, ujednolicone zasoby danych na poziomie krajowym, zarządzane przez NIH i ONC, aby przyspieszyć rozwój etycznej sztucznej inteligencji w medycynie.\",\n    \"Autoryzowano przeznaczenie 660 milionów dolarów na rok fiskalny 2025 na finansowanie tych działań, w tym na tworzenie zasobów obliczeniowych i edukację w zakresie AI.\"\n  ],\n  \"eng_ai_title\": \"Ethical AI Adoption in Healthcare: Data Consent and Research Funding.\",\n  \"eng_summary\": \"This bill authorizes significant funding to accelerate the ethical development of Artificial Intelligence in healthcare, aiming to improve medical treatment and research nationwide. Crucially, it establishes new rules requiring hospitals to ask patients for permission before sharing their electronic health records for AI research purposes. This ensures individuals maintain control over how their personal health data is utilized for scientific advancement.\",\n  \"eng_key_points\": [\n    \"Hospitals participating in Medicare must request patient permission to share Electronic Health Records (EHR) data for health-related research.\",\n    \"The law authorizes $660 million for Fiscal Year 2025 to fund federal agencies (NIH, ONC, NLM) to develop AI research resources and data standards.\",\n    \"New national data resources and interoperability standards will be established to unify access to clinical data for ethical biomedical AI research.\"\n  ],\n  \"de_ai_title\": \"Ethische KI im Gesundheitswesen: Patientenzustimmung und Forschungsförderung.\",\n  \"de_summary\": \"Dieses Gesetz genehmigt erhebliche Mittel, um die ethische Entwicklung der Künstlichen Intelligenz im Gesundheitswesen zu beschleunigen und die medizinische Versorgung zu verbessern. Eine wichtige Änderung ist die Verpflichtung für Krankenhäuser, Patienten um Erlaubnis zu bitten, bevor ihre elektronischen Gesundheitsdaten für KI-Forschungszwecke weitergegeben werden. Dies stärkt die Kontrolle der Bürger über ihre persönlichen Gesundheitsdaten.\",\n  \"de_key_points\": [\n    \"Krankenhäuser, die am Medicare-Programm teilnehmen, müssen Patienten um Erlaubnis bitten, ihre elektronischen Gesundheitsakten (EHR) für Forschungszwecke zu teilen.\",\n    \"Es werden 660 Millionen Dollar für das Geschäftsjahr 2025 bereitgestellt, um Bundesbehörden (NIH, ONC) bei der Entwicklung von KI-Forschungsressourcen und Datenstandards zu unterstützen.\",\n    \"Es werden neue nationale Datenressourcen und Interoperabilitätsstandards geschaffen, um den Zugang zu klinischen Daten für ethische biomedizinische KI-Forschung zu vereinheitlichen.\"\n  ],\n  \"fr_ai_title\": \"Adoption éthique de l'IA en santé: consentement des données et financement de la recherche.\",\n  \"fr_summary\": \"Ce projet de loi autorise un financement important pour accélérer le développement éthique de l'Intelligence Artificielle dans les soins de santé, visant à améliorer le traitement médical. Un changement clé pour les citoyens est l'obligation pour les hôpitaux de demander la permission des patients avant de partager leurs dossiers de santé électroniques à des fins de recherche en IA. Cela garantit que les individus gardent le contrôle sur l'utilisation de leurs données de santé personnelles.\",\n  \"fr_key_points\": [\n    \"Les hôpitaux participant à Medicare doivent demander l'autorisation des patients pour partager leurs dossiers de santé électroniques (DSE) à des fins de recherche.\",\n    \"660 millions de dollars sont autorisés pour l'exercice 2025 afin de financer les agences fédérales (NIH, ONC) pour développer des ressources de recherche en IA et des normes de données.\",\n    \"De nouvelles ressources nationales de données et des normes d'interopérabilité seront établies pour unifier l'accès aux données cliniques pour la recherche biomédicale éthique.\"\n  ],\n  \"es_ai_title\": \"Adopción ética de IA en salud: consentimiento de datos y financiación de investigación.\",\n  \"es_summary\": \"Esta legislación autoriza una financiación sustancial para impulsar el desarrollo ético de la Inteligencia Artificial en la atención médica, con el objetivo de mejorar los tratamientos. Un cambio fundamental para los ciudadanos es que los hospitales deberán solicitar permiso a los pacientes antes de compartir sus registros de salud electrónicos para la investigación con IA. Esto asegura que las personas mantengan el control sobre cómo se utilizan sus datos personales de salud.\",\n  \"es_key_points\": [\n    \"Los hospitales que participan en Medicare deben solicitar permiso al paciente para compartir los datos de sus Registros de Salud Electrónicos (RSE) con fines de investigación.\",\n    \"Se autorizan 660 millones de dólares para el año fiscal 2025 para financiar agencias federales (NIH, ONC) en el desarrollo de recursos de investigación de IA y estándares de datos.\",\n    \"Se establecerán nuevos recursos nacionales de datos y estándares de interoperabilidad para unificar el acceso a la información clínica para la investigación biomédica ética.\"\n  ],\n  \"it_ai_title\": \"Adozione etica dell'IA nella sanità: consenso sui dati e finanziamento della ricerca.\",\n  \"it_summary\": \"Questo disegno di legge autorizza finanziamenti significativi per accelerare lo sviluppo etico dell'Intelligenza Artificiale nel settore sanitario, mirando a migliorare i trattamenti medici. Un cambiamento cruciale per i cittadini è l'obbligo per gli ospedali di chiedere il permesso ai pazienti prima di condividere le loro cartelle cliniche elettroniche per scopi di ricerca sull'IA. Ciò garantisce che gli individui mantengano il controllo sull'utilizzo dei propri dati sanitari personali.\",\n  \"it_key_points\": [\n    \"Gli ospedali che partecipano a Medicare devono richiedere il permesso del paziente per condividere i dati delle cartelle cliniche elettroniche (EHR) per scopi di ricerca sanitaria.\",\n    \"Sono autorizzati 660 milioni di dollari per l'anno fiscale 2025 per finanziare le agenzie federali (NIH, ONC) nello sviluppo di risorse di ricerca sull'IA e standard di dati.\",\n    \"Verranno istituite nuove risorse nazionali di dati e standard di interoperabilità per unificare l'accesso ai dati clinici per la ricerca biomedica etica.\"\n  ],\n  \"nl_ai_title\": \"Ethische AI in de gezondheidszorg: toestemming voor gegevens en onderzoek financiering.\",\n  \"nl_summary\": \"Dit wetsvoorstel autoriseert aanzienlijke financiering om de ethische ontwikkeling van Kunstmatige Intelligentie in de gezondheidszorg te versnellen, met als doel de medische behandeling te verbeteren. Een cruciale verandering voor burgers is de verplichting voor ziekenhuizen om patiënten om toestemming te vragen voordat hun elektronische medische dossiers worden gedeeld voor AI-onderzoek. Dit zorgt ervoor dat individuen controle behouden over hoe hun persoonlijke gezondheidsgegevens worden gebruikt.\",\n  \"nl_key_points\": [\n    \"Ziekenhuizen die deelnemen aan Medicare moeten patiënttoestemming vragen om Elektronische Gezondheidsdossiers (EGD) te delen voor gezondheidsgerelateerde onderzoeksdoeleinden.\",\n    \"Er is 660 miljoen dollar geautoriseerd voor het fiscale jaar 2025 om federale instanties (NIH, ONC) te financieren voor de ontwikkeling van AI-onderzoeksbronnen en datastandaarden.\",\n    \"Nieuwe nationale gegevensbronnen en interoperabiliteitsstandaarden zullen worden vastgesteld om de toegang tot klinische gegevens voor ethisch biomedisch AI-onderzoek te verenigen.\"\n  ],\n  \"pt_ai_title\": \"Adoção ética de IA na saúde: consentimento de dados e financiamento de pesquisa.\",\n  \"pt_summary\": \"Este projeto de lei autoriza financiamento significativo para acelerar o desenvolvimento ético da Inteligência Artificial nos cuidados de saúde, visando melhorar o tratamento médico. Uma mudança crucial para os cidadãos é a obrigação de os hospitais solicitarem permissão aos pacientes antes de partilharem os seus registos de saúde eletrónicos para fins de pesquisa de IA. Isto garante que os indivíduos mantêm o controlo sobre a utilização dos seus dados pessoais de saúde.\",\n  \"pt_key_points\": [\n    \"Os hospitais participantes no Medicare devem solicitar a permissão do paciente para partilhar dados de Registos Eletrónicos de Saúde (RES) para fins de investigação.\",\n    \"Estão autorizados 660 milhões de dólares para o ano fiscal de 2025 para financiar agências federais (NIH, ONC) no desenvolvimento de recursos de pesquisa de IA e padrões de dados.\",\n    \"Novos recursos nacionais de dados e padrões de interoperabilidade serão estabelecidos para unificar o acesso a dados clínicos para pesquisa biomédica ética.\"\n  ],\n  \"category\": [\n    \"Health\",\n    \"Informatization\"\n  ]\n}"
    }
  ]
}