Notice: Function _load_textdomain_just_in_time was called incorrectly. Translation loading for the interactive-geo-maps domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /var/www/html/wp-includes/functions.php on line 6260 Notice: Function _load_textdomain_just_in_time was called incorrectly. Translation loading for the interactive-geo-maps domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /var/www/html/wp-includes/functions.php on line 6260 {"id":14795,"date":"2023-03-21T15:07:02","date_gmt":"2023-03-21T19:07:02","guid":{"rendered":"https:\/\/www.systechone.com\/?page_id=14795"},"modified":"2025-11-17T10:37:50","modified_gmt":"2025-11-17T15:37:50","slug":"pharmaceutical-compliance","status":"publish","type":"page","link":"https:\/\/systech.dev.ssdev.ca\/de\/solutions\/regulatory-compliance\/pharmaceutical-compliance\/","title":{"rendered":"PHARMAZEUTISCHE COMPLIANCE"},"content":{"rendered":"
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Zuhause<\/a><\/span><\/span><\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Einhaltung pharmazeutischer Vorschriften... Wir verstehen, was es braucht<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Systech bietet leistungsstarke Serialisierungs- und R\u00fcckverfolgbarkeitsfunktionen, die Sie bei der Einhaltung der weltweiten pharmazeutischen Vorschriften unterst\u00fctzen.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Umfassende, konfigurierbare, vollwertige L\u00f6sungen<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Unsere bew\u00e4hrte Softwareplattform deckt das gesamte Spektrum ab - von Stufe 1 bis Stufe 5 - und sorgt so f\u00fcr eine unschlagbar einfache Implementierung und schnelle Einhaltung der Vorschriften. Ger\u00e4teunabh\u00e4ngige, konfigurierbare L\u00f6sungen geben Ihnen die Flexibilit\u00e4t, sich an neue Einhaltung von Pharmaregeln<\/a> Anforderungen kosteneffizient zu erf\u00fcllen, ohne bei jeder \u00c4nderung eine Anpassung vornehmen zu m\u00fcssen, egal wo Sie t\u00e4tig sind.<\/span><\/p>

Die Einhaltung von Vorschriften erfordert eine Datengenauigkeit, die die physische Produktbewegung von der Herstellung bis zur Ausgabe widerspiegelt. Unsere Komplettl\u00f6sung erm\u00f6glicht einen nahtlosen und sicheren Datenaustausch f\u00fcr R\u00fcckverfolgbarkeit<\/a> \u00fcber die gesamte Lieferkette hinweg. In Kombination mit der M\u00f6glichkeit, eine Verbindung zu Stammdatensystemen und regulatorischen Datenbanken herzustellen, entsteht so ein konformes Aufzeichnungssystem f\u00fcr Ihre Produkte.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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DSCSA-Bereitschaft: Unterst\u00fctzung der Pharmaindustrie bei der Einhaltung\n<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Ein aktuelles Beispiel ist die letzte <\/span>DSCSA<\/span><\/a> Meilenstein, der die Einf\u00fchrung eines elektronischen, interoperablen Systems zur R\u00fcckverfolgung verschreibungspflichtiger Arzneimittel auf Packungsebene bis November 2024 vorschreibt. Diese erweiterten Sicherheitsanforderungen f\u00fcr den Arzneimittelvertrieb wirken sich auf das gesamte \u00d6kosystem der pharmazeutischen Lieferkette aus: <\/span>Hersteller<\/span><\/a>, Verteiler, <\/span>Spender<\/span><\/a>Umverpacker, <\/span>3PLs<\/span><\/a> und ihre Handelspartner. Systech unterst\u00fctzt Sie bei der Einhaltung von DSCSA, einschlie\u00dflich unserer <\/span>Verifizierungs-Router-Dienst (VRS)<\/span><\/a> und die Unterst\u00fctzung von autorisierten Handelspartnern (ATP), die eine vollst\u00e4ndige Einhaltung der pharmazeutischen Vorschriften gew\u00e4hrleisten.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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EU FMD: Vereinfachung der Einhaltung der Vorschriften f\u00fcr Pharmaunternehmen<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Die Richtlinie zur F\u00e4lschung von Arzneimitteln (FMD)<\/a> erfordert ein System von Repositories f\u00fcr Arzneimittelhersteller, um Produktinformationen und Seriennummern an die EU-Mitgliedstaaten zu \u00fcbermitteln. Systech vereinfacht diesen Prozess und hilft Ihnen dabei, bei der Abgabe von Arzneimitteln in ganz Europa die Einhaltung der Arzneimittelvorschriften zu gew\u00e4hrleisten.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tErfahren Sie mehr \u00fcber die EU-MKS<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Einhaltung der Vorschriften f\u00fcr klinische Studien<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Druck und \u00dcberpr\u00fcfung von Etiketten f\u00fcr Pr\u00fcfpr\u00e4parate (IMPs), die in klinische Studien<\/a> ist eine Herausforderung. Doch wenn es um die Sicherheit der Probanden, die Einhaltung gesetzlicher Vorschriften, die Nachverfolgung und die Integrit\u00e4t der Daten aus klinischen Studien geht, ist kein Platz f\u00fcr Kennzeichnungsfehler.\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tErfahren Sie mehr \u00fcber imps<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Ben\u00f6tigen Sie Hilfe bei der Einhaltung von Vorschriften in der Pharmaindustrie?<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Mit leistungsstarken Serialisierungs- und R\u00fcckverfolgbarkeitsfunktionen unterst\u00fctzen wir Sie bei der Einhaltung globaler Pharmavorschriften. Sprechen Sie jetzt mit einem Compliance-Experten!<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tLOS GEHT\u2018S<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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MEHR ERFAHREN<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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BLOGARTIKEL<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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F\u00fcr Apotheken beginnt die Einhaltung des DSCSA mit dem autorisierten Handel<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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In der sich schnell entwickelnden pharmazeutischen Landschaft ist die Einhaltung von Vorschriften f\u00fcr Apotheken von gr\u00f6\u00dfter Bedeutung.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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WEITERLESEN<\/a><\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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BLOGARTIKEL<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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DSCSA-Interoperabilit\u00e4tsfrist: Ist Ihre Organisation bereit?<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Systech und Vantage er\u00f6rtern, was erforderlich ist, um bis November 2023, dem letzten...<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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WEITERLESEN<\/a><\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Infografik<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Elektronische Beglaubigung: Wie man autorisierte Handelspartner einrichtet<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Die Einf\u00fchrung von Berechtigungsnachweisen durch autorisierte Handelspartner ist der Schl\u00fcssel zur Produktr\u00fcckverfolgung im Rahmen des DSCSA f\u00fcr 2023.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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DOWNLOAD hier<\/a><\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

Pharmaceutical compliance… We understand what it takes Systech offers powerful serialization and traceability functionality to help you meet global pharmaceutical regulatory compliance. Comprehensive, configurable, full-stack solutions Our proven software platform covers the full stack\u2014from Level 1 to Level 5\u2014for unbeatable ease of implementation and speed to compliance. Equipment-agnostic, configurable solutions give you flexibility to adapt […]<\/p>\n","protected":false},"author":20,"featured_media":0,"parent":15017,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"content-stage":[],"content-type":[],"conversation-track":[],"product-category":[],"class_list":["post-14795","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nAchieve Pharma Regulatory Compliance with Systech's Serialization Solutions<\/title>\n<meta name=\"description\" content=\"Ensure global pharma regulatory compliance with Systech\u2019s powerful serialization and traceability solutions for DSCSA, EU FMD, and clinical trials.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/staging.systech.ssdev.ca\/solutions\/regulatory-compliance\/pharmaceutical-compliance\/\" \/>\n<meta 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