{"id":25862,"date":"2026-01-12T12:49:57","date_gmt":"2026-01-12T11:49:57","guid":{"rendered":"https:\/\/cefi.es\/?p=25862"},"modified":"2026-01-27T09:52:26","modified_gmt":"2026-01-27T08:52:26","slug":"numero-95-de-cuadernos-de-derecho-farmaceutico","status":"publish","type":"post","link":"https:\/\/cefi.es\/%F0%9D%97%A1%F0%9D%98%82%F0%9D%97%BA%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%BC-%F0%9D%9F%B5%F0%9D%9F%B1-%F0%9D%97%B1%F0%9D%97%B2-%F0%9D%97%96%F0%9D%98%82%F0%9D%97%AE%F0%9D%97%B1%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%BB%F0%9D%97%BC%F0%9D%98%80-%F0%9D%97%B1%F0%9D%97%B2-%F0%9D%97%97%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%B2%F0%9D%97%B0%F0%9D%97%B5%F0%9D%97%BC-%F0%9D%97%99%F0%9D%97%AE%F0%9D%97%BF%F0%9D%97%BA%F0%9D%97%AE%F0%9D%97%B0%F0%9D%97%B2%F0%9D%98%82%F0%9D%98%81%F0%9D%97%B6%F0%9D%97%B0%F0%9D%97%BC\/","title":{"rendered":"N\u00famero 95 de Cuadernos de Derecho Farmac\u00e9utico"},"content":{"rendered":"\n<p>En el n\u00famero de Cuadernos de Derecho Farmac\u00e9utico que presentamos se abordan aspectos de actualidad muy interesantes. Desde la perspectiva de la interacci\u00f3n entre la normativa de productos sanitarios y la IA se analizan los requisitos impuestos en la normativa respecto a la seguridad, transparencia, gobernanza de datos y supervisi\u00f3n humana de los sistemas de inteligencia artificial que formen parte de un producto sanitario, as\u00ed como los problemas pr\u00e1cticos de estos sistemas.<br><br>Se analiza la reciente \ud835\udde6\ud835\uddf2\ud835\uddfb\ud835\ude01\ud835\uddf2\ud835\uddfb\ud835\uddf0\ud835\uddf6\ud835\uddee \ud835\uddf1\ud835\uddf2\ud835\uddf9 \ud835\udde7\ud835\uddff\ud835\uddf6\ud835\uddef\ud835\ude02\ud835\uddfb\ud835\uddee\ud835\uddf9 \ud835\uddf1\ud835\uddf2 \ud835\udddd\ud835\ude02\ud835\ude00\ud835\ude01\ud835\uddf6\ud835\uddf0\ud835\uddf6\ud835\uddee \ud835\uddf1\ud835\uddf2 \ud835\uddf9\ud835\uddee \ud835\udde8\ud835\uddfb\ud835\uddf6\ud835\uddfc\u0301\ud835\uddfb \ud835\uddd8\ud835\ude02\ud835\uddff\ud835\uddfc\ud835\uddfd\ud835\uddf2\ud835\uddee \ud835\uddf1\ud835\uddf2 \ud835\udfed\ud835\udff5 \ud835\uddf1\ud835\uddf2 \ud835\uddf7\ud835\ude02\ud835\uddfb\ud835\uddf6\ud835\uddfc \ud835\uddf1\ud835\uddf2 \ud835\udfee\ud835\udfec\ud835\udfee\ud835\udff1, dictada en el asunto C-200\/24, en la que se declara que una prohibici\u00f3n absoluta de promoci\u00f3n de oficinas de farmacia impuesta por un Estado miembro es contraria al Derecho de la Uni\u00f3n. Se pone en el contexto de la jurisprudencia europea entre publicidad de medicamentos y publicidad de oficinas de farmacia y se reflexiona sobre el posible impacto de la sentencia en la normativa espa\u00f1ola de ordenaci\u00f3n farmac\u00e9utica.<br><br>Otro de los art\u00edculos de este n\u00famero, aborda los conflictos de inter\u00e9s en el sector farmac\u00e9utico destacando su complejidad. Se hace un an\u00e1lisis en detalle las diferentes definiciones y enfoques y se recomienda establecer una pol\u00edtica de compliance robusta, basada en la evaluaci\u00f3n, identificaci\u00f3n, resoluci\u00f3n y monitorizaci\u00f3n continua de los conflictos de inter\u00e9s.<br><br>As\u00ed mismo, se comenta la propuesta de un Biotech Act europeo que representa una oportunidad para superar los obst\u00e1culos del sector biotecnol\u00f3gico: fragmentaci\u00f3n normativa, procesos cl\u00ednicos desalineados, falta de capital y pol\u00edticas inconsistentes que amenazan con frenar la innovaci\u00f3n y desplazarla hacia regiones m\u00e1s favorables. Destacan como prioridades armonizar los ensayos cl\u00ednicos, simplificar regulaciones para productos combinados, reforzar la capacidad t\u00e9cnica de los reguladores, eliminar duplicidades en control de calidad, mejorar el acceso a financiaci\u00f3n y avanzar en la integraci\u00f3n de datos de salud y herramientas de IA. Estas reformas y la necesaria adaptaci\u00f3n de las estrategias nacionales, contribuir\u00e1 a que Europa recupere su liderazgo en este campo y a acelerar el acceso de los pacientes a nuevas terapias.<br><br>Por \u00faltimo, este n\u00famero contiene una breve rese\u00f1a de la 20\u00aa Edici\u00f3n de nuestro Curso de Derecho Farmac\u00e9utico.<br><br>\ud83d\udc49 <a href=\"https:\/\/app.cefi.es\/publicacion\/2025-cuadernos-95\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/app.cefi.es\/publicacion\/2025-cuadernos-95<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"594\" height=\"841\" src=\"https:\/\/cefi.es\/wp-contenido\/uploads\/2026\/01\/Captura-de-pantalla-2026-01-12-a-las-12.44.34.png\" alt=\"\" class=\"wp-image-25865\" srcset=\"https:\/\/cefi.es\/wp-contenido\/uploads\/2026\/01\/Captura-de-pantalla-2026-01-12-a-las-12.44.34.png 594w, https:\/\/cefi.es\/wp-contenido\/uploads\/2026\/01\/Captura-de-pantalla-2026-01-12-a-las-12.44.34-212x300.png 212w\" sizes=\"auto, (max-width: 594px) 100vw, 594px\" \/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>En el n\u00famero de Cuadernos de Derecho Farmac\u00e9utico que presentamos se abordan aspectos de actualidad muy interesantes. Desde la perspectiva de la interacci\u00f3n entre la normativa de productos sanitarios y la IA se analizan los requisitos impuestos en la normativa respecto a la seguridad, transparencia, gobernanza de datos y supervisi\u00f3n humana de los sistemas de [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":25863,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-25862","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-sin-categoria"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>N\u00famero 95 de Cuadernos de Derecho Farmac\u00e9utico - Centro de estudios para el fomento de la investigaci\u00f3n<\/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:\/\/cefi.es\/en\/%F0%9D%97%A1%F0%9D%98%82%F0%9D%97%BA%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%BC-%F0%9D%9F%B5%F0%9D%9F%B1-%F0%9D%97%B1%F0%9D%97%B2-%F0%9D%97%96%F0%9D%98%82%F0%9D%97%AE%F0%9D%97%B1%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%BB%F0%9D%97%BC%F0%9D%98%80-%F0%9D%97%B1%F0%9D%97%B2-%F0%9D%97%97%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%B2%F0%9D%97%B0%F0%9D%97%B5%F0%9D%97%BC-%F0%9D%97%99%F0%9D%97%AE%F0%9D%97%BF%F0%9D%97%BA%F0%9D%97%AE%F0%9D%97%B0%F0%9D%97%B2%F0%9D%98%82%F0%9D%98%81%F0%9D%97%B6%F0%9D%97%B0%F0%9D%97%BC\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"N\u00famero 95 de Cuadernos de Derecho Farmac\u00e9utico - Centro de estudios para el fomento de la investigaci\u00f3n\" \/>\n<meta property=\"og:description\" content=\"En el n\u00famero de Cuadernos de Derecho Farmac\u00e9utico que presentamos se abordan aspectos de actualidad muy interesantes. Desde la perspectiva de la interacci\u00f3n entre la normativa de productos sanitarios y la IA se analizan los requisitos impuestos en la normativa respecto a la seguridad, transparencia, gobernanza de datos y supervisi\u00f3n humana de los sistemas de [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/cefi.es\/%F0%9D%97%A1%F0%9D%98%82%F0%9D%97%BA%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%BC-%F0%9D%9F%B5%F0%9D%9F%B1-%F0%9D%97%B1%F0%9D%97%B2-%F0%9D%97%96%F0%9D%98%82%F0%9D%97%AE%F0%9D%97%B1%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%BB%F0%9D%97%BC%F0%9D%98%80-%F0%9D%97%B1%F0%9D%97%B2-%F0%9D%97%97%F0%9D%97%B2%F0%9D%97%BF%F0%9D%97%B2%F0%9D%97%B0%F0%9D%97%B5%F0%9D%97%BC-%F0%9D%97%99%F0%9D%97%AE%F0%9D%97%BF%F0%9D%97%BA%F0%9D%97%AE%F0%9D%97%B0%F0%9D%97%B2%F0%9D%98%82%F0%9D%98%81%F0%9D%97%B6%F0%9D%97%B0%F0%9D%97%BC\/\" \/>\n<meta property=\"og:site_name\" content=\"Centro de estudios para el fomento de la investigaci\u00f3n\" \/>\n<meta property=\"article:published_time\" 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