{"id":5687,"date":"2025-09-15T08:30:00","date_gmt":"2025-09-15T08:30:00","guid":{"rendered":"https:\/\/pharmanomos.ch\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/"},"modified":"2026-04-28T06:07:02","modified_gmt":"2026-04-28T06:07:02","slug":"swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler","status":"publish","type":"post","link":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/","title":{"rendered":"Swissmedic Regulatory News 2025: Leitfaden f\u00fcr Apotheken, Importeure und Gro\u00dfh\u00e4ndler"},"content":{"rendered":"\n<h2 class=\"wp-block-heading has-large-font-size\">Swissdamed &#8211; Modul UDI-Ger\u00e4te<\/h2>\n\n<p class=\"has-medium-font-size\">Ab dem <strong>18. August 2025<\/strong> hat Swissmedic das Modul <strong>UDI Devices<\/strong> in der <strong>Swissdamed-Datenbank<\/strong> aktiviert, das die freiwillige Registrierung von Medizinprodukten, IVDs und Kit\/Process Packs (SPPs) erm\u00f6glicht.<br\/>Ab dem <strong>1. Juli 2026<\/strong> wird die Registrierung jedoch <strong>f\u00fcr alle in der Schweiz in Verkehr gebrachten Produkte obligatorisch<\/strong>.<br\/>Es wird auch eine kurze \u00dcbergangsfrist bis zum <strong>31. Dezember 2026<\/strong> geben <a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/swissdamed-informationen\/registrierung-mepprodukte-moeglich.html?utm_source=chatgpt.com\" target=\"_blank\" rel=\"noreferrer noopener\">swissmedic.ch+2swissmedic.ch+2<\/a>.<br\/><strong>Wichtig<\/strong>: Wenn ein Produkt von einer Feldsicherheitskorrekturma\u00dfnahme (FSCA) betroffen ist, gibt es <strong>keinen \u00dcbergang<\/strong>: die Registrierung erfolgt sofort ab dem 1. Juli 2026.<\/p>\n\n<p class=\"has-small-font-size\">F\u00fcr weitere Informationen:<\/p>\n\n<ul class=\"wp-block-list link-verde has-small-font-size\">\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/swissdamed-informationen\/registrierung-mepprodukte-moeglich.html\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/swissdamed-informationen\/registrierung-mepprodukte-moeglich.html<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/produktregistrierung.html\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/produktregistrierung.html<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/faq.html\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/faq.html<\/a><\/li>\n<\/ul>\n\n<h2 class=\"wp-block-heading has-large-font-size\">eIFU (Elektronische Gebrauchsanweisung)<\/h2>\n\n<p class=\"has-medium-font-size\">Am <strong>8. August 2025<\/strong> setzte Swissmedic die EU-Verordnung 2025\/1234 um und dehnte die Verwendung <strong>elektronischer Gebrauchsanweisungen<\/strong><em>(eIFUs)<\/em> auch auf die Schweiz aus, sofern sie f\u00fcr Fachleute bestimmt sind.<br\/><strong>Gebrauchsanweisungen, die f\u00fcr die breite \u00d6ffentlichkeit<\/strong> (z.B. Patienten) <strong>bestimmt sind<\/strong>, m\u00fcssen weiterhin in Papierform vorliegen.<br\/>Der Link zu eIFUs muss in der UDI-Datenbank registriert werden.<\/p>\n\n<p class=\"has-small-font-size\">F\u00fcr weitere Informationen:<\/p>\n\n<ul class=\"wp-block-list link-verde has-small-font-size\">\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/regulation-of-medical-devices\/anwendbare-rechtsakte-gemaess-eu-mdr\/umsetzung-eu-durchfuehrungsverordnung-gebrauchsanweisungen.html?utm_source=chatgpt.com\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/regulation-of-medical-devices\/anwendbare-rechtsakte-gemaess-eu-mdr\/umsetzung-eu-durchfuehrungsverordnung-gebrauchsanweisungen.html<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/medenvoyglobal.com\/blog\/new-eu-regulation-on-eifus-adopted-by-swissmedic\/\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/medenvoyglobal.com\/blog\/new-eu-regulation-on-eifus-adopted-by-swissmedic\/<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.swiss-medtech.ch\/en\/news\/eifu-regulation-switzerland\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swiss-medtech.ch\/en\/news\/eifu-regulation-switzerland<\/a><\/li>\n<\/ul>\n\n<h2 class=\"wp-block-heading has-large-font-size\"><strong>R\u00fcckverfolgbarkeitssystem (Swissdamed &#8211; Registrierung von Akteuren und Ger\u00e4ten)<\/strong><\/h2>\n\n<p class=\"has-medium-font-size\">Das Swissdamed System besteht aus zwei Hauptteilen:<\/p>\n\n<ul class=\"wp-block-list has-medium-font-size\">\n<li class=\"has-medium-font-size\"><strong>Akteursmodul<\/strong> (aktiv ab August 2024): Register der Wirtschaftsbeteiligten (Hersteller, Bevollm\u00e4chtigte, Montagebetriebe).<\/li>\n\n\n\n<li><strong>UDI-Ger\u00e4te-Modul<\/strong> (aktiviert ab August 2025): Register von Ger\u00e4ten und IVDs, die f\u00fcr den Schweizer Markt bestimmt sind.<\/li>\n<\/ul>\n\n<p class=\"has-medium-font-size\">Sie werden aufgefordert, das <strong>Wirtschaftsprofil<\/strong> (Akteur) zu erstellen, bevor Sie mit der Registrierung des Ger\u00e4ts beginnen.<\/p>\n\n<p class=\"has-small-font-size\">F\u00fcr weitere Informationen:<\/p>\n\n<ul class=\"wp-block-list link-verde has-small-font-size\">\n<li><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/medenvoyglobal.com\/blog\/swissmedic-rolls-out-new-swissdamed-udi-devices-module\/\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/medenvoyglobal.com\/blog\/swissmedic-rolls-out-new-swissdamed-udi-devices-module\/<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/cmcmedicaldevices.com\/swissdamed-udi-devices-module-medical-device-registration-now-available\/\" target=\"_blank\" rel=\"noopener\" title=\"\">https:\/\/cmcmedicaldevices.com\/swissdamed-udi-devices-module-medical-device-registration-now-available\/<\/a><\/li>\n<\/ul>\n\n<h2 class=\"wp-block-heading has-large-font-size\">Richtlinien f\u00fcr SPP &#8211; Systems and Procedure Packs<\/h2>\n\n<p class=\"has-medium-font-size\">Im Jahr <strong>2025<\/strong> wurde ein Informationsdokument zur Angleichung der Schweizer Vorschriften an die EU-Vorschriften (MDR\/IVDR) f\u00fcr <strong>PWS<\/strong> ver\u00f6ffentlicht. Diejenigen, die diese Produkte herstellen und vermarkten, sind verpflichtet, sich innerhalb von <strong>drei Monaten<\/strong> nach dem ersten Inverkehrbringen registrieren zu lassen. Die Verpflichtung umfasst auch die <strong>\u00dcberwachung nach dem Inverkehrbringen<\/strong>.  <a href=\"https:\/\/www.pureglobal.com\/news\/swissmedic-2025-guidance-on-systems-and-procedure-packs?utm_source=chatgpt.com\" target=\"_blank\" rel=\"noreferrer noopener\"><\/a><\/p>\n\n<p class=\"has-small-font-size\">F\u00fcr weitere Informationen:<\/p>\n\n<ul class=\"wp-block-list has-small-font-size\">\n<li class=\"link-verde\"><a href=\"https:\/\/www.pureglobal.com\/news\/swissmedic-2025-guidance-on-systems-and-procedure-packs\">https:\/\/www.pureglobal.com\/news\/swissmedic-2025-guidance-on-systems-and-procedure-packs<\/a><\/li>\n<\/ul>\n\n<h2 class=\"wp-block-heading has-large-font-size\">Operative Zusammenfassung (Tabelle)<\/h2>\n\n<figure class=\"wp-block-table link-verde\"><table class=\"has-fixed-layout\"><thead><tr><th class=\"has-text-align-left\" data-align=\"left\">Thema<\/th><th class=\"has-text-align-left\" data-align=\"left\">Schl\u00fcssel Verfallsdatum<\/th><th class=\"has-text-align-left\" data-align=\"left\">Verpflichtend<\/th><th class=\"has-text-align-left\" data-align=\"left\">Offizielle Links<\/th><\/tr><\/thead><tbody><tr><td class=\"has-text-align-left\" data-align=\"left\">UDI-Ger\u00e4te (Swissdamed)<\/td><td class=\"has-text-align-left\" data-align=\"left\">Obligatorisch ab 1\/7\/2026<\/td><td class=\"has-text-align-left\" data-align=\"left\">Hersteller, Vertreter, Assemblierer<br\/><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/swissdamed-informationen\/registrierung-mepprodukte-moeglich.html?utm_source=chatgpt.com\" target=\"_blank\" rel=\"noreferrer noopener\"><\/a><\/td><td class=\"has-text-align-left\" data-align=\"left\"><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank\/swissdamed-informationen\/registrierung-mepprodukte-moeglich.html\" target=\"_blank\" rel=\"noopener\" title=\"Link 1\">Link 1<\/a> und <a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/medizinprodukte-datenbank.html\" target=\"_blank\" rel=\"noopener\" title=\"Link 2\">Link 2<\/a><\/td><\/tr><tr><td class=\"has-text-align-left\" data-align=\"left\">eIFU (elektronisch)<\/td><td class=\"has-text-align-left\" data-align=\"left\">Aktiv ab 8\/8\/2025<\/td><td class=\"has-text-align-left\" data-align=\"left\">Aufzunehmende Hersteller UDI URL<br\/><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/regulation-of-medical-devices\/anwendbare-rechtsakte-gemaess-eu-mdr\/umsetzung-eu-durchfuehrungsverordnung-gebrauchsanweisungen.html?utm_source=chatgpt.com\" target=\"_blank\" rel=\"noreferrer noopener\"><\/a><\/td><td class=\"has-text-align-left\" data-align=\"left\"><a href=\"https:\/\/www.swissmedic.ch\/swissmedic\/en\/home\/medical-devices\/regulation-of-medical-devices\/anwendbare-rechtsakte-gemaess-eu-mdr\/umsetzung-eu-durchfuehrungsverordnung-gebrauchsanweisungen.html\" target=\"_blank\" rel=\"noopener\" title=\"Link 1\">Link 1<\/a> und <a href=\"https:\/\/medenvoyglobal.com\/blog\/new-eu-regulation-on-eifus-adopted-by-swissmedic\/\" target=\"_blank\" rel=\"noopener\" title=\"\">Link 2<\/a><\/td><\/tr><tr><td class=\"has-text-align-left\" data-align=\"left\">SPP<\/td><td class=\"has-text-align-left\" data-align=\"left\">Registrierung innerhalb von 3 Monaten<\/td><td class=\"has-text-align-left\" data-align=\"left\">SPP-Monteure<br\/><a href=\"https:\/\/www.pureglobal.com\/news\/swissmedic-2025-guidance-on-systems-and-procedure-packs?utm_source=chatgpt.com\" target=\"_blank\" rel=\"noreferrer noopener\"><\/a><\/td><td class=\"has-text-align-left\" data-align=\"left\"><a href=\"https:\/\/www.pureglobal.com\/news\/swissmedic-2025-guidance-on-systems-and-procedure-packs\" target=\"_blank\" rel=\"noopener\" title=\"\">Link 1<\/a><\/td><\/tr><\/tbody><\/table><\/figure>\n\n<h2 class=\"wp-block-heading has-large-font-size\">Auswirkungen f\u00fcr Apotheken, Importeure und Gro\u00dfh\u00e4ndler<\/h2>\n\n<p class=\"has-medium-font-size\"><strong>Apotheken<\/strong>: Sie sollten nur dann eine Registrierung beantragen, wenn sie als SPP-Assemblierer t\u00e4tig sind; ansonsten ist es wichtig, insbesondere bei Zubereitungen, auf eIFU und ter-Compliance vorbereitet zu sein.<\/p>\n\n<p class=\"has-medium-font-size\"><strong>Importeure<\/strong>: Sie m\u00fcssen bei Swissdamed als &#8222;Akteur&#8220; registriert sein, der mit den importierten Ger\u00e4ten in Verbindung steht, k\u00f6nnen aber die Ger\u00e4te selbst nicht registrieren; dies ist das Vorrecht des Herstellers oder seines Bevollm\u00e4chtigten.<\/p>\n\n<p class=\"has-medium-font-size\"><strong>Gro\u00dfh\u00e4ndler\/Vertreiber<\/strong>: m\u00fcssen R\u00fcckverfolgbarkeit und UDI-Anpassung sicherstellen, aber die Registrierung wird dem Hauptakteur \u00fcberlassen. Die Verwendung von eIFU und die Teilnahme an der \u00dcberwachung sind entscheidend. <\/p>\n\n<h2 class=\"wp-block-heading has-large-font-size\">Warum Hilfe holen?<\/h2>\n\n<p class=\"has-medium-font-size\">Diese \u00c4nderungen erfordern eine <strong>proaktive Planung<\/strong>, insbesondere f\u00fcr Importeure, Hersteller und Apotheken, die sich mit der R\u00fcckverfolgbarkeit von SPP, der \u00dcberwachung oder der Montage besch\u00e4ftigen. Mit technischer oder operativer Unterst\u00fctzung k\u00f6nnen wir Ihre aktuellen Verfahren anpassen, um <strong>die Einhaltung der Vorschriften zu gew\u00e4hrleisten<\/strong>. <\/p>\n\n<div class=\"wp-block-uagb-buttons uagb-buttons__outer-wrap uagb-btn__default-btn uagb-btn-tablet__default-btn uagb-btn-mobile__default-btn uagb-block-e038fb4f\"><div class=\"uagb-buttons__wrap uagb-buttons-layout-wrap \">\n<div class=\"wp-block-uagb-buttons-child uagb-buttons__outer-wrap uagb-block-80a1dd4c wp-block-button\"><div class=\"uagb-button__wrapper\"><a class=\"uagb-buttons-repeater wp-block-button__link\" aria-label=\"\" href=\"mailto:info@pharmanomos.ch\" rel=\"follow noopener\" target=\"_self\" role=\"button\"><div class=\"uagb-button__link\">Kontaktieren Sie uns jetzt<\/div><\/a><\/div><\/div>\n<\/div><\/div>\n\n<p class=\"has-medium-font-size\"><em><strong>Kostenlose Beratung!<\/strong><\/em><\/p>\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Swissdamed &#8211; Modul UDI-Ger\u00e4te Ab dem 18. August 2025 hat Swissmedic das Modul UDI Devices in der Swissdamed-Datenbank aktiviert, das die freiwillige Registrierung von Medizinprodukten, IVDs und Kit\/Process Packs (SPPs) erm\u00f6glicht.Ab dem 1. Juli 2026 wird die Registrierung jedoch f\u00fcr alle in der Schweiz in Verkehr gebrachten Produkte obligatorisch.Es wird auch eine kurze \u00dcbergangsfrist bis [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":5176,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[15],"tags":[],"class_list":["post-5687","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-nicht-kategorisiert"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Swissmedic Regulatory News 2025: UDI, eIFU und Swissdamed<\/title>\n<meta name=\"description\" content=\"Leitfaden zu Swissmedic 2025: UDI-Registrierung in Swissdamed, elektronische eIFUs, R\u00fcckverfolgbarkeit und Pflichten f\u00fcr Apotheken und Importeure .\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Swissmedic Regulatory News 2025: UDI, eIFU und Swissdamed\" \/>\n<meta property=\"og:description\" content=\"Leitfaden zu Swissmedic 2025: UDI-Registrierung in Swissdamed, elektronische eIFUs, R\u00fcckverfolgbarkeit und Pflichten f\u00fcr Apotheken und Importeure .\" \/>\n<meta property=\"og:url\" content=\"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/\" \/>\n<meta property=\"og:site_name\" content=\"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera\" \/>\n<meta property=\"article:published_time\" content=\"2025-09-15T08:30:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2026-04-28T06:07:02+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" \/>\n\t<meta property=\"og:image:height\" content=\"900\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"giuseppe.cantoni.marketer@gmail.com\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Verfasst von\" \/>\n\t<meta name=\"twitter:data1\" content=\"giuseppe.cantoni.marketer@gmail.com\" \/>\n\t<meta name=\"twitter:label2\" content=\"Gesch\u00e4tzte Lesezeit\" \/>\n\t<meta name=\"twitter:data2\" content=\"3\u00a0Minuten\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/\"},\"author\":{\"name\":\"giuseppe.cantoni.marketer@gmail.com\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#\\\/schema\\\/person\\\/63997ce71a35d3b996aaa2af93f1fa71\"},\"headline\":\"Swissmedic Regulatory News 2025: Leitfaden f\u00fcr Apotheken, Importeure und Gro\u00dfh\u00e4ndler\",\"datePublished\":\"2025-09-15T08:30:00+00:00\",\"dateModified\":\"2026-04-28T06:07:02+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/\"},\"wordCount\":601,\"publisher\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/pharmanomos.ch\\\/wp-content\\\/uploads\\\/2025\\\/09\\\/Immagini-per-Blog-news.png\",\"articleSection\":[\"Nicht kategorisiert\"],\"inLanguage\":\"de\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/\",\"url\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/\",\"name\":\"Swissmedic Regulatory News 2025: UDI, eIFU und Swissdamed\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/pharmanomos.ch\\\/wp-content\\\/uploads\\\/2025\\\/09\\\/Immagini-per-Blog-news.png\",\"datePublished\":\"2025-09-15T08:30:00+00:00\",\"dateModified\":\"2026-04-28T06:07:02+00:00\",\"description\":\"Leitfaden zu Swissmedic 2025: UDI-Registrierung in Swissdamed, elektronische eIFUs, R\u00fcckverfolgbarkeit und Pflichten f\u00fcr Apotheken und Importeure .\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#breadcrumb\"},\"inLanguage\":\"de\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"de\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#primaryimage\",\"url\":\"https:\\\/\\\/pharmanomos.ch\\\/wp-content\\\/uploads\\\/2025\\\/09\\\/Immagini-per-Blog-news.png\",\"contentUrl\":\"https:\\\/\\\/pharmanomos.ch\\\/wp-content\\\/uploads\\\/2025\\\/09\\\/Immagini-per-Blog-news.png\",\"width\":1200,\"height\":900},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Swissmedic Regulatory News 2025: Leitfaden f\u00fcr Apotheken, Importeure und Gro\u00dfh\u00e4ndler\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#website\",\"url\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/\",\"name\":\"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera\",\"description\":\"Soluzioni su misura per la gestione della qualit\u00e0 nelle farmacie. Consulenza specializzata, documentazione digitale e area clienti riservata.\",\"publisher\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"de\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#organization\",\"name\":\"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera\",\"url\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"de\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/pharmanomos.ch\\\/wp-content\\\/uploads\\\/2025\\\/05\\\/cropped-Logo-Pharmanomos-1-1.png\",\"contentUrl\":\"https:\\\/\\\/pharmanomos.ch\\\/wp-content\\\/uploads\\\/2025\\\/05\\\/cropped-Logo-Pharmanomos-1-1.png\",\"width\":766,\"height\":300,\"caption\":\"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera\"},\"image\":{\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\"},\"sameAs\":[\"https:\\\/\\\/www.linkedin.com\\\/company\\\/pharmanomos-sagl\\\/\"]},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/pharmanomos.ch\\\/en\\\/#\\\/schema\\\/person\\\/63997ce71a35d3b996aaa2af93f1fa71\",\"name\":\"giuseppe.cantoni.marketer@gmail.com\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"de\",\"@id\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/86b45b79a7c5cbaa8ca0bac39a5abc2ab5a88326e9adb469614a07550afd15c8?s=96&d=mm&r=g\",\"url\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/86b45b79a7c5cbaa8ca0bac39a5abc2ab5a88326e9adb469614a07550afd15c8?s=96&d=mm&r=g\",\"contentUrl\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/86b45b79a7c5cbaa8ca0bac39a5abc2ab5a88326e9adb469614a07550afd15c8?s=96&d=mm&r=g\",\"caption\":\"giuseppe.cantoni.marketer@gmail.com\"},\"sameAs\":[\"https:\\\/\\\/pharmanomos.ch\"],\"url\":\"https:\\\/\\\/pharmanomos.ch\\\/de\\\/author\\\/giuseppe-cantoni-marketergmail-com\\\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Swissmedic Regulatory News 2025: UDI, eIFU und Swissdamed","description":"Leitfaden zu Swissmedic 2025: UDI-Registrierung in Swissdamed, elektronische eIFUs, R\u00fcckverfolgbarkeit und Pflichten f\u00fcr Apotheken und Importeure .","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/","og_locale":"de_DE","og_type":"article","og_title":"Swissmedic Regulatory News 2025: UDI, eIFU und Swissdamed","og_description":"Leitfaden zu Swissmedic 2025: UDI-Registrierung in Swissdamed, elektronische eIFUs, R\u00fcckverfolgbarkeit und Pflichten f\u00fcr Apotheken und Importeure .","og_url":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/","og_site_name":"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera","article_published_time":"2025-09-15T08:30:00+00:00","article_modified_time":"2026-04-28T06:07:02+00:00","og_image":[{"width":1200,"height":900,"url":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png","type":"image\/png"}],"author":"giuseppe.cantoni.marketer@gmail.com","twitter_card":"summary_large_image","twitter_misc":{"Verfasst von":"giuseppe.cantoni.marketer@gmail.com","Gesch\u00e4tzte Lesezeit":"3\u00a0Minuten"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#article","isPartOf":{"@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/"},"author":{"name":"giuseppe.cantoni.marketer@gmail.com","@id":"https:\/\/pharmanomos.ch\/en\/#\/schema\/person\/63997ce71a35d3b996aaa2af93f1fa71"},"headline":"Swissmedic Regulatory News 2025: Leitfaden f\u00fcr Apotheken, Importeure und Gro\u00dfh\u00e4ndler","datePublished":"2025-09-15T08:30:00+00:00","dateModified":"2026-04-28T06:07:02+00:00","mainEntityOfPage":{"@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/"},"wordCount":601,"publisher":{"@id":"https:\/\/pharmanomos.ch\/en\/#organization"},"image":{"@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#primaryimage"},"thumbnailUrl":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png","articleSection":["Nicht kategorisiert"],"inLanguage":"de"},{"@type":"WebPage","@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/","url":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/","name":"Swissmedic Regulatory News 2025: UDI, eIFU und Swissdamed","isPartOf":{"@id":"https:\/\/pharmanomos.ch\/en\/#website"},"primaryImageOfPage":{"@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#primaryimage"},"image":{"@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#primaryimage"},"thumbnailUrl":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png","datePublished":"2025-09-15T08:30:00+00:00","dateModified":"2026-04-28T06:07:02+00:00","description":"Leitfaden zu Swissmedic 2025: UDI-Registrierung in Swissdamed, elektronische eIFUs, R\u00fcckverfolgbarkeit und Pflichten f\u00fcr Apotheken und Importeure .","breadcrumb":{"@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#breadcrumb"},"inLanguage":"de","potentialAction":[{"@type":"ReadAction","target":["https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/"]}]},{"@type":"ImageObject","inLanguage":"de","@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#primaryimage","url":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png","contentUrl":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png","width":1200,"height":900},{"@type":"BreadcrumbList","@id":"https:\/\/pharmanomos.ch\/de\/swissmedic-regulatory-news-2025-leitfaden-fuer-apotheken-importeure-und-grosshaendler\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/pharmanomos.ch\/de\/"},{"@type":"ListItem","position":2,"name":"Swissmedic Regulatory News 2025: Leitfaden f\u00fcr Apotheken, Importeure und Gro\u00dfh\u00e4ndler"}]},{"@type":"WebSite","@id":"https:\/\/pharmanomos.ch\/en\/#website","url":"https:\/\/pharmanomos.ch\/en\/","name":"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera","description":"Soluzioni su misura per la gestione della qualit\u00e0 nelle farmacie. Consulenza specializzata, documentazione digitale e area clienti riservata.","publisher":{"@id":"https:\/\/pharmanomos.ch\/en\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/pharmanomos.ch\/en\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"de"},{"@type":"Organization","@id":"https:\/\/pharmanomos.ch\/en\/#organization","name":"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera","url":"https:\/\/pharmanomos.ch\/en\/","logo":{"@type":"ImageObject","inLanguage":"de","@id":"https:\/\/pharmanomos.ch\/en\/#\/schema\/logo\/image\/","url":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/05\/cropped-Logo-Pharmanomos-1-1.png","contentUrl":"https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/05\/cropped-Logo-Pharmanomos-1-1.png","width":766,"height":300,"caption":"Pharmanomos Sagl \u2013 Consulenza e Sistemi Qualit\u00e0 per Farmacie in Svizzera"},"image":{"@id":"https:\/\/pharmanomos.ch\/en\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/www.linkedin.com\/company\/pharmanomos-sagl\/"]},{"@type":"Person","@id":"https:\/\/pharmanomos.ch\/en\/#\/schema\/person\/63997ce71a35d3b996aaa2af93f1fa71","name":"giuseppe.cantoni.marketer@gmail.com","image":{"@type":"ImageObject","inLanguage":"de","@id":"https:\/\/secure.gravatar.com\/avatar\/86b45b79a7c5cbaa8ca0bac39a5abc2ab5a88326e9adb469614a07550afd15c8?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/86b45b79a7c5cbaa8ca0bac39a5abc2ab5a88326e9adb469614a07550afd15c8?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/86b45b79a7c5cbaa8ca0bac39a5abc2ab5a88326e9adb469614a07550afd15c8?s=96&d=mm&r=g","caption":"giuseppe.cantoni.marketer@gmail.com"},"sameAs":["https:\/\/pharmanomos.ch"],"url":"https:\/\/pharmanomos.ch\/de\/author\/giuseppe-cantoni-marketergmail-com\/"}]}},"uagb_featured_image_src":{"full":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png",1200,900,false],"thumbnail":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news-150x150.png",150,150,true],"medium":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news-300x225.png",300,225,true],"medium_large":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news-768x576.png",768,576,true],"large":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news-1024x768.png",1024,768,true],"1536x1536":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png",1200,900,false],"2048x2048":["https:\/\/pharmanomos.ch\/wp-content\/uploads\/2025\/09\/Immagini-per-Blog-news.png",1200,900,false]},"uagb_author_info":{"display_name":"giuseppe.cantoni.marketer@gmail.com","author_link":"https:\/\/pharmanomos.ch\/de\/author\/giuseppe-cantoni-marketergmail-com\/"},"uagb_comment_info":0,"uagb_excerpt":"Swissdamed &#8211; Modul UDI-Ger\u00e4te Ab dem 18. August 2025 hat Swissmedic das Modul UDI Devices in der Swissdamed-Datenbank aktiviert, das die freiwillige Registrierung von Medizinprodukten, IVDs und Kit\/Process Packs (SPPs) erm\u00f6glicht.Ab dem 1. Juli 2026 wird die Registrierung jedoch f\u00fcr alle in der Schweiz in Verkehr gebrachten Produkte obligatorisch.Es wird auch eine kurze \u00dcbergangsfrist bis&hellip;","_links":{"self":[{"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/posts\/5687","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/comments?post=5687"}],"version-history":[{"count":1,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/posts\/5687\/revisions"}],"predecessor-version":[{"id":5690,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/posts\/5687\/revisions\/5690"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/media\/5176"}],"wp:attachment":[{"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/media?parent=5687"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/categories?post=5687"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/pharmanomos.ch\/de\/wp-json\/wp\/v2\/tags?post=5687"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}