{"id":29668,"date":"2024-05-15T08:53:28","date_gmt":"2024-05-15T06:53:28","guid":{"rendered":"https:\/\/www.hollandbio.nl\/?p=29668"},"modified":"2024-05-15T08:53:29","modified_gmt":"2024-05-15T06:53:29","slug":"bereid-je-voor-op-de-eu-hta-regulation","status":"publish","type":"post","link":"https:\/\/www.hollandbio.nl\/en\/nieuws\/bereid-je-voor-op-de-eu-hta-regulation\/","title":{"rendered":"Bereid je voor op de EU HTA Regulation"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Op 12 januari 2025 gaat er veel veranderen rond de vergoeding van nieuwe geneesmiddelen. Vanaf dan moeten alle nieuwe oncologische geneesmiddelen en ATMP\u2019s bij het aanvragen van een marktvergunning bij de EMA gelijktijdig een Joint Clinical Assessment procedure doorlopen, als eerste stap van het vergoedingsproces. In Nederland bereidt het Zorginstituut zich voor op deze nieuwe wetgeving. Benieuwd hoe het ZIN dit doet, en wat je als bedrijf kan doen om je voor te bereiden? Houd dan <a href=\"https:\/\/www.zorginstituutnederland.nl\/werkagenda\/overige-onderwerpen\/eu-htar\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>deze pagina<\/strong><\/a> in de gaten. \u00a0<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Op 12 januari 2025 gaat er veel veranderen rond de vergoeding van nieuwe geneesmiddelen. Vanaf dan moeten alle nieuwe oncologische geneesmiddelen en ATMP\u2019s bij het aanvragen van een marktvergunning bij de EMA gelijktijdig een Joint Clinical Assessment procedure doorlopen, als eerste stap van het vergoedingsproces. In Nederland bereidt het Zorginstituut zich voor op deze nieuwe [&hellip;]<\/p>\n","protected":false},"author":20,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[39],"tags":[],"class_list":["post-29668","post","type-post","status-publish","format-standard","hentry","category-gezondheid"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.0 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Bereid je voor op de EU HTA Regulation - hollandbio<\/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.hollandbio.nl\/en\/nieuws\/bereid-je-voor-op-de-eu-hta-regulation\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Bereid je voor op de EU HTA Regulation - hollandbio\" \/>\n<meta property=\"og:description\" content=\"Op 12 januari 2025 gaat er veel veranderen rond de vergoeding van nieuwe geneesmiddelen. Vanaf dan moeten alle nieuwe oncologische geneesmiddelen en ATMP\u2019s bij het aanvragen van een marktvergunning bij de EMA gelijktijdig een Joint Clinical Assessment procedure doorlopen, als eerste stap van het vergoedingsproces. 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