{"id":7950,"date":"2025-01-08T20:33:04","date_gmt":"2025-01-08T12:33:04","guid":{"rendered":"https:\/\/regask.com\/?p=7950"},"modified":"2025-01-08T20:33:04","modified_gmt":"2025-01-08T12:33:04","slug":"us-amerikanische-fda-konferenz-zu-kinderarzneimitteln","status":"publish","type":"post","link":"https:\/\/regask.com\/de\/us-fda-pediatric-drug-meeting\/","title":{"rendered":"US-amerikanische FDA k\u00fcndigt \u00f6ffentliche Sitzung zur Gesetzgebung f\u00fcr Kinderarzneimittel an \u2026"},"content":{"rendered":"<p>Der <strong><a href=\"https:\/\/regask.com\/de\/patientenzentrierte-arzneimittelentwicklung-der-fda\/\">Lebensmittel- und Arzneimittelbeh\u00f6rde<\/a> (FDA)<\/strong> hat eine \u00f6ffentliche Versammlung mit dem Titel <strong>\u201eTreffen interessierter Kreise: Umsetzung des Best Pharmaceuticals for Children Act (BPCA) und des Paediatric Research Equity Act (PREA)\u201c<\/strong> An <strong>15. Mai 2025<\/strong>. Diese Veranstaltung bietet den Beteiligten eine Plattform, um die Auswirkungen der Kinderheilkundegesetzgebung auf die Arzneimittel- und Biologikaentwicklung zu diskutieren und so zuk\u00fcnftige Fortschritte in der Kindergesundheitsversorgung zu gestalten.<\/p>\n<h4><strong>Ziele des Meetings:<\/strong><\/h4>\n<p>Die FDA bittet um Input von verschiedenen Interessengruppen \u2013 darunter Patientengruppen, Pflegekr\u00e4fte, Industrievertreter und Wissenschaftler \u2013 um:<\/p>\n<ol>\n<li><strong>Auswirkungen auf die \u00f6ffentliche Gesundheit bewerten:<\/strong> Untersuchen Sie, wie BPCA und PREA die Behandlungsm\u00f6glichkeiten f\u00fcr Kinder beeinflusst und ungedeckte medizinische Bed\u00fcrfnisse angegangen haben.<\/li>\n<li><strong>Ausgleich von Anreizen und Anforderungen:<\/strong> Informieren Sie sich dar\u00fcber, wie sich Anreize im Rahmen des BPCA und Studienmandate im Rahmen des PREA auf Pl\u00e4ne zur Arzneimittelentwicklung auswirken.<\/li>\n<li><strong>Barrieren identifizieren:<\/strong> Besprechen Sie Herausforderungen wie die Infrastruktur f\u00fcr klinische Studien, die Vielfalt der Teilnehmer und H\u00fcrden, die den Abschluss der Studie verhindern.<\/li>\n<li><strong>Nutzen Sie wissenschaftliche Fortschritte:<\/strong> Heben Sie innovative Ans\u00e4tze wie p\u00e4diatrische Extrapolation, adaptive Studiendesigns, Biomarker als Ersatz und Echtzeitdaten hervor, um die Beweisf\u00fchrung f\u00fcr p\u00e4diatrische Populationen zu verbessern.<\/li>\n<li><strong>Globale Ausrichtung verbessern:<\/strong> Gehen Sie auf die Bedeutung der internationalen Zusammenarbeit bei der Entwicklung von Kinderarzneimitteln ein.<\/li>\n<\/ol>\n<h4><strong>Veranstaltungsdetails:<\/strong><\/h4>\n<ul>\n<li><strong>Datum:<\/strong> 15. Mai 2025<\/li>\n<li><strong>Zeit:<\/strong> 9:00 \u2013 16:30 Uhr Eastern Time<\/li>\n<li><strong>Standort:<\/strong>\n<ul>\n<li><strong>Praktisch<\/strong><\/li>\n<li><strong>Vor Ort:<\/strong> FDA White Oak Campus, 10903 New Hampshire Ave., Geb\u00e4ude 31 Konferenzzentrum, White Oak Great Room, Silver Spring, MD 20993-0002<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h4><strong>So nehmen Sie teil:<\/strong><\/h4>\n<ul>\n<li>Interessenvertreter werden ermutigt, an dem Treffen teilzunehmen und ihre Erfahrungen in Bezug auf BPCA und PREA auszutauschen.<\/li>\n<li>Elektronische oder schriftliche Kommentare zur Sitzung m\u00fcssen eingereicht werden bis <strong>13. Juni 2025<\/strong>.<\/li>\n<\/ul>\n<h4><strong>Auswirkungen auf die Entwicklung von Arzneimitteln f\u00fcr Kinder:<\/strong><\/h4>\n<p>Diese \u00f6ffentliche Veranstaltung wird die Strategien f\u00fcr die Entwicklung von Kinderarzneimitteln und Biologika beeinflussen und dabei Bereiche mit hohem medizinischem Bedarf hervorheben. Der Fokus der FDA auf die Nutzung fortschrittlicher wissenschaftlicher Methoden wie Realweltdaten, adaptiver Studien und p\u00e4diatrischer Extrapolation bietet den Beteiligten die M\u00f6glichkeit, ihre Entwicklungspl\u00e4ne an die sich entwickelnden regulatorischen Erwartungen anzupassen.<\/p>\n<p>Dieses Treffen spiegelt die <a href=\"https:\/\/regask.com\/de\/fda-zulassung-fur-medizinprodukte-iron-man-ahnliche-schnittstelle\/\">Verpflichtung der FDA<\/a> zur Weiterentwicklung der Kindergesundheitsversorgung durch Zusammenarbeit, Innovation und robuste regulatorische Rahmenbedingungen.<\/p>","protected":false},"excerpt":{"rendered":"<p>Die Food and Drug Administration (FDA) hat f\u00fcr den 15. Mai 2025 eine \u00f6ffentliche Sitzung mit dem Titel \u201cTreffen interessierter Parteien: Umsetzung des Best Pharmaceuticals for Children Act (BPCA) und des Paediatric Research Equity Act (PREA)\u201d anberaumt. Diese Veranstaltung bietet Interessenvertretern eine Plattform, um die Auswirkungen der p\u00e4diatrischen Gesetzgebung auf die Entwicklung von Arzneimitteln und Biologika zu diskutieren und\u2026<\/p>","protected":false},"author":30,"featured_media":7955,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[527,35],"tags":[617,165],"class_list":["post-7950","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-united-states-regulations","category-pharma-biotech-latest-insights","tag-biologics-regulation","tag-public-health"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.3 (Yoast SEO v27.5) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>US FDA to Host Meeting on Pediatric Drug Development | RegASK<\/title>\n<meta name=\"description\" content=\"US FDA announces a public meeting on pediatric drug development, focusing on BPCA, &amp; PREA. 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