{"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\/es\/blog\/another-successful-fda-audit-in-the-books","title":{"rendered":"Otra auditor\u00eda exitosa de la FDA en los libros"},"content":{"rendered":"

Recientemente, Augmentir complet\u00f3 una rigurosa auditor\u00eda de calificaci\u00f3n de proveedores como parte de las Buenas Pr\u00e1cticas de Fabricaci\u00f3n (GMP) de una empresa de fabricaci\u00f3n farmac\u00e9utica de nivel 1, y nos complace anunciar que nuestro producto pas\u00f3 la auditor\u00eda con \u00e9xito.<\/span><\/p>\n

Seg\u00fan el <\/span>Sociedad Internacional de Ingenier\u00eda Farmac\u00e9utica<\/span><\/a>Las regulaciones GMP exigen que los fabricantes farmac\u00e9uticos controlen adecuadamente las operaciones de fabricaci\u00f3n y establezcan un enfoque de calidad para la fabricaci\u00f3n, lo que permite a las empresas minimizar o eliminar los casos de contaminaci\u00f3n, confusiones y errores. El uso del software de trabajador conectado de Augmentir es un componente fundamental para la fabricaci\u00f3n dentro de... ciencias farmac\u00e9uticas y de la vida<\/a> medio ambiente, ya que ayuda a reducir errores y garantiza el cumplimiento de estas regulaciones.<\/span><\/p>\n

Esta auditor\u00eda de calificaci\u00f3n, realizada por el Auditor Principal y el Especialista S\u00e9nior en Validaci\u00f3n de Control de Calidad de nuestro cliente, evalu\u00f3 la idoneidad y eficacia para el cumplimiento de los requisitos regulatorios. Tambi\u00e9n se evaluaron la calidad, eficacia y cumplimiento del Sistema de Gesti\u00f3n de Calidad (SGC), las pol\u00edticas y los procedimientos de la planta, y finalmente, Augmentir fue aprobado como Proveedor de Sistemas\/Infraestructura de TI Empresarial.\u00a0<\/span><\/p>\n

Auditor\u00edas como estas suponen un reto para cualquier empresa y pueden representar desaf\u00edos a\u00fan mayores para peque\u00f1as empresas como Augmentir. Sin embargo, son de suma importancia, ya que las normas GMP garantizan un enfoque de calidad en la fabricaci\u00f3n, ayudando a las empresas a minimizar errores y casos de contaminaci\u00f3n.\u00a0\u00a0<\/span><\/p>\n

En Augmentir, hemos completado con \u00e9xito m\u00faltiples auditor\u00edas hasta la fecha y nos complace a\u00f1adir esta auditor\u00eda de BPM farmac\u00e9utica a esa lista, a medida que continuamos con el desarrollo de nuestros productos tradicionales. Estas auditor\u00edas no son nuevas para nuestro equipo, y este reciente hito es una continuaci\u00f3n de... <\/span>Nuestra historia en la introducci\u00f3n de software innovador y de alta calidad en el sector manufacturero<\/span><\/a>habiendo realizado m\u00e1s de 100.000 procesos auditados a lo largo de la historia de los productos de software en los que nuestro equipo ha participado.<\/span><\/p>\n

Al comenzar el a\u00f1o 2022, esta finalizaci\u00f3n de la auditor\u00eda de GMP farmac\u00e9utica es un testimonio de Augmentir, nuestro equipo y nuestro compromiso de mantener los m\u00e1s altos est\u00e1ndares de calidad global y valida nuestro \u00e9xito en la industria farmac\u00e9utica.\u00a0<\/span><\/p>\n

\u00a1Por nuestra pr\u00f3xima auditor\u00eda exitosa!<\/span><\/p>\n

 <\/p>","protected":false},"excerpt":{"rendered":"

Recientemente, Augmentir complet\u00f3 una rigurosa auditor\u00eda de calificaci\u00f3n como parte de las Buenas Pr\u00e1cticas de Fabricaci\u00f3n (GMP) de una empresa de fabricaci\u00f3n farmac\u00e9utica de nivel 1, y nos complace anunciar que nuestro producto pas\u00f3 la auditor\u00eda con \u00e9xito.<\/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":"\nAnother Successful FDA Audit in the Books - Augmentir<\/title>\n<meta name=\"description\" content=\"Recently, Augmentir completed a rigorous quality audit as part of a Tier 1 Pharmaceutical Manufacturing company\u2019s Good Manufacturing Practice (GMP), and we are pleased to announce that our product successfully passed the audit.\" \/>\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.augmentir.com\/es\/blog\/another-successful-fda-audit-in-the-books\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Another Successful FDA Audit in the Books - 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