{"id":155921,"date":"2025-01-15T03:00:27","date_gmt":"2025-01-15T02:00:27","guid":{"rendered":"https:\/\/www.cde.ual.es\/?p=155921"},"modified":"2025-01-14T09:12:15","modified_gmt":"2025-01-14T08:12:15","slug":"the-eu-facilitates-access-to-healthcare-innovation-with-new-rules","status":"publish","type":"post","link":"https:\/\/www.cde.ual.es\/en\/the-eu-facilitates-access-to-healthcare-innovation-with-new-rules\/","title":{"rendered":"The EU facilitates access to healthcare innovation with new rules"},"content":{"rendered":"<p style=\"text-align: justify;\">On Sunday, 12 January, the\u00a0Regulation on Health Technology Assessment\u00a0(HTA) will become applicable, bringing a significant improvement in\u00a0ensuring that innovative and effective health technologies are available to patients across the EU.<\/p>\n<p><a href=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2025\/01\/laboratory-2815641_1280.jpg\"><img decoding=\"async\" class=\"wp-image-155919 aligncenter\" src=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2025\/01\/laboratory-2815641_1280.jpg\" alt=\"\" width=\"828\" height=\"552\" srcset=\"https:\/\/www.cde.ual.es\/wp-content\/uploads\/2025\/01\/laboratory-2815641_1280.jpg 1280w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2025\/01\/laboratory-2815641_1280-300x200.jpg 300w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2025\/01\/laboratory-2815641_1280-1024x682.jpg 1024w, https:\/\/www.cde.ual.es\/wp-content\/uploads\/2025\/01\/laboratory-2815641_1280-768x512.jpg 768w\" sizes=\"(max-width: 828px) 100vw, 828px\" \/><\/a><\/p>\n<p style=\"text-align: justify;\">The new rules create an EU framework for the assessment of health technologies, such as medicines and medical devices, by fostering collaboration and coordination between EU Member States. This will help national authorities to make more timely and informed decisions on the pricing and reimbursement of health technologies and streamline the procedure for health technology developers. This will contribute to\u00a0faster and wider access to new and more effective innovative products for patients.<\/p>\n<p style=\"text-align: justify;\">The rules will apply to companies seeking marketing authorisation for their products by introducing a\u00a0new and permanent EU framework\u00a0for Health Technology Assessment, including through:<\/p>\n<ul style=\"text-align: justify;\" type=\"disc\">\n<li>introducing a single EU-level submission file for joint clinical assessments\u00a0in order to ensure\u00a0pooling of resources at the EU level\u00a0and\u00a0strengthening the scientific quality of HTA\u00a0across the EU whileavoiding duplication of assessments at national level.<\/li>\n<li>establishing faster procedures\u00a0requiring Joint Clinical Assessments to be completed within 30 days after the authorisation of the medicine;<\/li>\n<li>the\u00a0systematic consultation of patients and clinicians\u00a0during the preparation of the assessments as well as the involvement and consultation of the HTA stakeholders.<\/li>\n<\/ul>\n<p style=\"text-align: justify;\">As a first step, starting on 12 January, these new rules will apply to marketing authorisation applications for a\u00a0new cancer medicine or an advanced therapy medicinal product\u00a0(ATMP). The rules will be\u00a0extended to orphan medicines in January 2028\u00a0and will as of\u00a02030 cover all new medicinal products. Selected\u00a0high-risk medical devices\u00a0will also be assessed as of 2026.<\/p>\n<p style=\"text-align: justify;\">The new EU framework replaces the long standing \u00a0EU-funded project-based cooperation between Member States on health technology assessment, while fully respecting Member States&#8217; responsibility for the management of their health services as their national context requires.<\/p>\n<p style=\"text-align: justify;\">Background<\/p>\n<p style=\"text-align: justify;\">Health technology assessment is a scientific, evidence-based process that aims to inform the creation of safe and effective health policies by summarising information about the medical, social, economic and ethical issues related to the use of a health technology.<\/p>\n<p style=\"text-align: justify;\">The European Commission adopted its proposal for a Regulation on Health Technology Assessment on 31 January 2018. Adopted in December 2021, the Regulation, a key deliverable of the\u00a0EU Pharmaceutical Strategy, entered into force in January 2022. It applies from 12 January 2025. During this three-year transitional period, the Commission and the Member States prepared by seting up the necessary governance structure and drafted preparatory documents to support an effective application.<\/p>\n<p>&nbsp;<\/p>\n<p>More information <a href=\"https:\/\/ec.europa.eu\/commission\/presscorner\/detail\/en\/ip_25_226\">Commission European.\u00a0<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>On Sunday, 12 January, the\u00a0Regulation on Health Technology Assessment\u00a0(HTA) will become applicable, bringing a significant improvement in\u00a0ensuring that innovative and effective health technologies are available to patients across the EU. The new rules create an EU framework for the assessment of health technologies, such as medicines and medical devices, by fostering collaboration and coordination between [&hellip;]<\/p>\n","protected":false},"author":101011,"featured_media":155919,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":""},"categories":[4092,4096],"tags":[437,1502,13182],"class_list":{"0":"post-155921","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-health","8":"category-tech-prof-health","9":"tag-health","10":"tag-healthcare","11":"tag-medical-technology","12":"entry"},"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>The EU facilitates access to healthcare innovation with new rules | CDE Almer\u00eda - Centro de Documentaci\u00f3n Europea - Universidad de Almer\u00eda<\/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:\/\/www.cde.ual.es\/?p=155917\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The EU facilitates access to healthcare innovation with new rules | CDE Almer\u00eda - Centro de Documentaci\u00f3n Europea - Universidad de Almer\u00eda\" \/>\n<meta property=\"og:description\" content=\"On Sunday, 12 January, the\u00a0Regulation on Health Technology Assessment\u00a0(HTA) will become applicable, bringing a significant improvement in\u00a0ensuring that innovative and effective health technologies are available to patients across the EU. 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