{"id":12380,"date":"2022-02-08T19:56:11","date_gmt":"2022-02-08T19:56:11","guid":{"rendered":"https:\/\/www.augmentir.com\/?p=12380"},"modified":"2023-03-08T20:25:20","modified_gmt":"2023-03-08T20:25:20","slug":"another-successful-fda-audit-in-the-books","status":"publish","type":"post","link":"https:\/\/www.augmentir.com\/fr\/blog\/another-successful-fda-audit-in-the-books","title":{"rendered":"Un autre audit r\u00e9ussi de la FDA dans les livres"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">R\u00e9cemment, Augmentir a r\u00e9alis\u00e9 un audit rigoureux de qualification des fournisseurs dans le cadre des bonnes pratiques de fabrication (BPF) d&#039;une entreprise de fabrication pharmaceutique de niveau 1, et nous sommes heureux d&#039;annoncer que notre produit a r\u00e9ussi l&#039;audit.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Selon le <\/span><a href=\"https:\/\/ispe.org\/initiatives\/regulatory-resources\/gmp\/what-is-gmp\"><span style=\"font-weight: 400;\">Soci\u00e9t\u00e9 internationale de g\u00e9nie pharmaceutique<\/span><\/a><span style=\"font-weight: 400;\">, les r\u00e9glementations GMP exigent que les fabricants de produits pharmaceutiques contr\u00f4lent de mani\u00e8re ad\u00e9quate les op\u00e9rations de fabrication et \u00e9tablissent une approche qualit\u00e9 de la fabrication, permettant aux entreprises de minimiser ou d&#039;\u00e9liminer les cas de contamination, de confusion et d&#039;erreurs. L&#039;utilisation du logiciel de travail connect\u00e9 d&#039;Augmentir est un \u00e9l\u00e9ment essentiel pour la fabrication au sein du <a href=\"https:\/\/www.augmentir.com\/industries\/pharmaceutical-and-life-sciences-manufacturing\">pharmaceutique et sciences de la vie<\/a> l&#039;environnement, car il contribue \u00e0 r\u00e9duire les erreurs et garantit le respect de ces r\u00e9glementations.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Cet audit de qualification, effectu\u00e9 par l&#039;auditeur principal de notre client et le sp\u00e9cialiste principal de la validation de l&#039;AQ, a \u00e9valu\u00e9 l&#039;ad\u00e9quation et l&#039;efficacit\u00e9 du respect et de la conformit\u00e9 aux exigences r\u00e9glementaires. La qualit\u00e9, l&#039;efficacit\u00e9 et la conformit\u00e9 au syst\u00e8me de gestion de la qualit\u00e9 (SMQ), aux politiques et aux proc\u00e9dures du site ont \u00e9galement \u00e9t\u00e9 \u00e9valu\u00e9es et, finalement, Augmentir a \u00e9t\u00e9 approuv\u00e9 en tant que fournisseur de syst\u00e8me informatique d&#039;entreprise\/d&#039;infrastructure.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Des audits comme ceux-ci sont difficiles pour toute entreprise et peuvent pr\u00e9senter des d\u00e9fis encore plus grands pour les petites entreprises comme Augmentir. Pourtant, il est extr\u00eamement important car les r\u00e9glementations GMP garantissent une approche de qualit\u00e9 de la fabrication, aidant les entreprises \u00e0 minimiser les erreurs, les fautes et les cas de contamination.\u00a0\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Chez Augmentir, nous avons r\u00e9alis\u00e9 avec succ\u00e8s plusieurs audits \u00e0 ce jour et nous sommes ravis d&#039;ajouter cet audit GMP pharmaceutique \u00e0 cette liste alors que nous poursuivons les \u00e9tapes de nos produits h\u00e9rit\u00e9s. Ces audits ne sont pas nouveaux pour notre \u00e9quipe, et cette \u00e9tape r\u00e9cente s&#039;inscrit dans la continuit\u00e9 de <\/span><a href=\"\/blog\/national-roots-day-a-history-of-manufacturing-software-innovation\"><span style=\"font-weight: 400;\">notre histoire dans l&#039;introduction de logiciels innovants et de haute qualit\u00e9 dans le secteur manufacturier<\/span><\/a><span style=\"font-weight: 400;\">, ayant r\u00e9alis\u00e9 plus de 100 000 processus audit\u00e9s estim\u00e9s tout au long de l&#039;histoire des produits logiciels dans lesquels notre \u00e9quipe a \u00e9t\u00e9 impliqu\u00e9e.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Alors que nous entamons 2022, cette r\u00e9alisation de l&#039;audit GMP pharmaceutique t\u00e9moigne d&#039;Augmentir, de notre \u00e9quipe et de notre engagement \u00e0 maintenir les normes de qualit\u00e9 mondiales les plus \u00e9lev\u00e9es et valide notre succ\u00e8s dans l&#039;industrie pharmaceutique.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u00c0 notre prochain audit r\u00e9ussi\u00a0!<\/span><\/p>\n<p>&nbsp;<\/p>","protected":false},"excerpt":{"rendered":"<p>R\u00e9cemment, Augmentir a r\u00e9alis\u00e9 un audit de qualification rigoureux dans le cadre des bonnes pratiques de fabrication (BPF) d&#039;une entreprise de fabrication pharmaceutique de niveau 1, et nous sommes heureux d&#039;annoncer que notre produit a r\u00e9ussi l&#039;audit.<\/p>","protected":false},"author":1,"featured_media":12381,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false,"_lmt_disableupdate":"no","_lmt_disable":"","footnotes":""},"categories":[4],"tags":[86,47,85,84,87,83,88],"class_list":["post-12380","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog","tag-audit","tag-connected-worker","tag-fda","tag-gmp","tag-pharmaceutical-manufacturing","tag-quality","tag-validated"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - 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