{"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:\/\/www.systechone.com\/fr\/solutions\/regulatory-compliance\/pharmaceutical-compliance\/","title":{"rendered":"Conformit\u00e9 pharmaceutique"},"content":{"rendered":"
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Accueil<\/a><\/span><\/span><\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Conformit\u00e9 pharmaceutique... Nous comprenons ce qu'il faut<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Systech offre de puissantes fonctionnalit\u00e9s de s\u00e9rialisation et de tra\u00e7abilit\u00e9 pour vous aider \u00e0 respecter les r\u00e9glementations pharmaceutiques internationales.<\/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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Des solutions compl\u00e8tes, configurables et \u00e0 part enti\u00e8re<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Notre plate-forme logicielle \u00e9prouv\u00e9e couvre l'ensemble du spectre - du niveau 1 au niveau 5 - pour une facilit\u00e9 de mise en \u0153uvre et une rapidit\u00e9 de mise en conformit\u00e9 imbattables. Les solutions configurables et agnostiques en mati\u00e8re d'\u00e9quipement vous offrent la souplesse n\u00e9cessaire pour vous adapter aux nouvelles technologies. conformit\u00e9 r\u00e9glementaire dans le secteur pharmaceutique<\/a> de mani\u00e8re rentable, sans avoir \u00e0 les adapter \u00e0 chaque changement, quel que soit l'endroit o\u00f9 vous exercez votre activit\u00e9.<\/span><\/p>

La conformit\u00e9 exige l'exactitude des donn\u00e9es qui refl\u00e8tent le mouvement physique du produit du point de fabrication au point de distribution. Notre solution compl\u00e8te permet un \u00e9change de donn\u00e9es transparent et s\u00e9curis\u00e9 pour tra\u00e7abilit\u00e9<\/a> tout au long de la cha\u00eene d'approvisionnement. Combin\u00e9 \u00e0 la possibilit\u00e9 de se connecter aux syst\u00e8mes de donn\u00e9es de r\u00e9f\u00e9rence et aux bases de donn\u00e9es r\u00e9glementaires, cela permet de cr\u00e9er un syst\u00e8me d'enregistrement conforme pour vos produits.<\/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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Pr\u00e9paration \u00e0 la DSCSA : Soutenir la conformit\u00e9 de l'industrie pharmaceutique\n<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Un exemple d'actualit\u00e9 est la finale de l'appel d'offres de l'Union europ\u00e9enne pour l'achat d'une voiture. <\/span>DSCSA<\/span><\/a> qui impose la mise en \u0153uvre d'un syst\u00e8me \u00e9lectronique interop\u00e9rable permettant de tracer les m\u00e9dicaments sur ordonnance au niveau de l'emballage d'ici \u00e0 novembre 2024. Ces exigences renforc\u00e9es en mati\u00e8re de s\u00e9curit\u00e9 de la distribution des m\u00e9dicaments ont un impact sur l'ensemble de l'\u00e9cosyst\u00e8me de la cha\u00eene d'approvisionnement pharmaceutique : <\/span>fabricants<\/span><\/a>, distributeurs, <\/span>distributeurs<\/span><\/a>les reconditionneurs, <\/span>3PL<\/span><\/a> et leurs partenaires commerciaux. Systech vous couvre pour la conformit\u00e9 DSCSA, y compris notre <\/span>Service de v\u00e9rification par routeur (VRS)<\/span><\/a> et des partenaires commerciaux agr\u00e9\u00e9s (ATP), garantissant une conformit\u00e9 totale avec les r\u00e9glementations pharmaceutiques.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Directive europ\u00e9enne sur la fi\u00e8vre aphteuse : simplifier la mise en conformit\u00e9 des entreprises pharmaceutiques<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Le Directive sur les m\u00e9dicaments falsifi\u00e9s (FMD)<\/a> exige un syst\u00e8me de d\u00e9p\u00f4ts pour les fabricants de produits pharmaceutiques afin d'envoyer les informations sur les produits et les num\u00e9ros de s\u00e9rie aux pays membres de l'UE. Systech simplifie ce processus, en vous aidant \u00e0 vous connecter et \u00e0 garantir la conformit\u00e9 aux r\u00e9glementations pharmaceutiques lorsque vous distribuez des m\u00e9dicaments \u00e0 travers l'Europe.<\/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\tEn savoir plus sur la fi\u00e8vre aphteuse dans l'UE<\/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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Conformit\u00e9 r\u00e9glementaire des essais cliniques<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Impression et v\u00e9rification des \u00e9tiquettes pour les m\u00e9dicaments exp\u00e9rimentaux (IMP) utilis\u00e9s dans le cadre de la recherche sur les maladies infectieuses. essais cliniques<\/a> est un d\u00e9fi. Mais avec la s\u00e9curit\u00e9 des sujets, la conformit\u00e9 r\u00e9glementaire, les besoins de suivi et de tra\u00e7abilit\u00e9 et l'int\u00e9grit\u00e9 des donn\u00e9es des essais cliniques en jeu, il n'y a pas de place pour les erreurs d'\u00e9tiquetage.\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\tEn savoir plus sur les 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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EN SAVOIR PLUS<\/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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PAGE DE BLOG<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Pour les pharmacies, la conformit\u00e9 \u00e0 la DSCSA commence par le commerce autoris\u00e9.<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Dans le paysage pharmaceutique en \u00e9volution rapide, le maintien de la conformit\u00e9 r\u00e9glementaire est primordial pour les pharmacies.<\/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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LIRE LA SUITE<\/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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PAGE DE BLOG<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Date limite d'interop\u00e9rabilit\u00e9 de la DSCSA : Votre organisation est-elle pr\u00eate ?<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Systech et Vantage discutent de ce qu'il faut faire pour \u00eatre conforme d'ici novembre 2023, la date...<\/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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LIRE LA SUITE<\/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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Infographie<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Titres de comp\u00e9tences \u00e9lectroniques : Comment \u00e9tablir des partenaires commerciaux autoris\u00e9s<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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La mise en \u0153uvre de l'accr\u00e9ditation par l'interm\u00e9diaire de partenaires commerciaux autoris\u00e9s est essentielle pour la tra\u00e7abilit\u00e9 des produits dans le cadre de la DSCSA pour 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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T\u00e9l\u00e9charger ici<\/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":"

Conformit\u00e9 pharmaceutique... Nous comprenons ce qu'il faut Systech offre de puissantes fonctionnalit\u00e9s de s\u00e9rialisation et de tra\u00e7abilit\u00e9 pour vous aider \u00e0 respecter la conformit\u00e9 r\u00e9glementaire pharmaceutique mondiale. Des solutions compl\u00e8tes et configurables Notre plateforme logicielle \u00e9prouv\u00e9e couvre l'ensemble de la cha\u00eene - du niveau 1 au niveau 5 - pour une facilit\u00e9 de mise en \u0153uvre et une rapidit\u00e9 de mise en conformit\u00e9 imbattables. Les solutions configurables et agnostiques en mati\u00e8re d'\u00e9quipement vous permettent de vous adapter [...]<\/p>","protected":false},"author":20,"featured_media":0,"parent":15017,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"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:\/\/www.systechone.com\/fr\/solutions\/regulatory-compliance\/pharmaceutical-compliance\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Achieve Pharma Regulatory Compliance with Systech's Serialization Solutions\" \/>\n<meta property=\"og:description\" content=\"Ensure global pharma regulatory compliance with Systech\u2019s powerful serialization and traceability solutions for DSCSA, EU FMD, and clinical trials.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.systechone.com\/fr\/solutions\/regulatory-compliance\/pharmaceutical-compliance\/\" \/>\n<meta property=\"og:site_name\" content=\"Systech\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/systechone\/\" \/>\n<meta property=\"article:modified_time\" content=\"2025-11-17T15:37:50+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.systechone.com\/wp-content\/uploads\/2024\/01\/compliance-graphic_750x849-v2.png\" \/>\n\t<meta property=\"og:image:width\" content=\"750\" \/>\n\t<meta property=\"og:image:height\" content=\"849\" 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