{"id":2226,"date":"2024-08-04T23:38:27","date_gmt":"2024-08-04T21:38:27","guid":{"rendered":"http:\/\/comnova.de\/website\/?page_id=2226"},"modified":"2025-05-20T02:45:12","modified_gmt":"2025-05-20T00:45:12","slug":"gmp-services-de","status":"publish","type":"page","link":"http:\/\/comnova.de\/website\/de\/leistungen\/gmp-services-de\/","title":{"rendered":"GMP \u2013 Services de"},"content":{"rendered":"\n<p class=\"has-text-color has-link-color wp-elements-a1176d26e4689e4343665207fb49a3ce\" style=\"color:#b81a1a;font-size:30px\">GMP \u2013 Services<\/p>\n\n\n\n<p class=\"has-text-color has-link-color has-medium-font-size wp-elements-acbe29243d9f57a8c196ffc5614d01aa\" style=\"color:#b81a1a\"><strong>Kompetente Umsetzung von GMP-Anforderungen<\/strong><\/p>\n\n\n\n<p>Der EU-GMP-Leitfaden (Good Manufacturing Practice) f\u00fcr Human- und Tierarzneimittel konfrontiert die Pharmabranche mit enormen Anforderungen. Diese zu erf\u00fcllen, ist ein Kraftakt in puncto Zeit und Ressourcen. \u00c4u\u00dferste Sorgfalt und fundiertes Fachwissen sind dabei Pflicht.<\/p>\n\n\n\n<p>Wir unterst\u00fctzen Sie professionell und kompetent bei der Umsetzung Ihrer GMP-Anforderungen, mit viel Liebe zum Detail. Die COMNOVA GmbH hat sich als Dienstleister f\u00fcr Qualifizierungs- und Validierungsma\u00dfnahmen in der Pharmaindustrie bei vielen Projekten bew\u00e4hrt. Fordern Sie unser Spezial-Know-how und unsere langj\u00e4hrige Erfahrung!<\/p>\n\n\n\n<p>Die COMNOVA GMP-Services umfassen:<\/p>\n\n\n\n<p>Erstellung von Qualifizierungs- und Validierungs-Dokumenten<\/p>\n\n\n\n<ul style=\"background-color:#f7f7f7\" class=\"wp-block-list has-background\">\n<li>Validierungsmasterplan<\/li>\n\n\n\n<li>Risikoanalysen<\/li>\n\n\n\n<li>Qualifizierungspl\u00e4ne<\/li>\n\n\n\n<li>Qualfizierungstestprotokolle<\/li>\n\n\n\n<li>Qualifizierungsberichte<\/li>\n\n\n\n<li>Umsetzung von Qualifizierungsma\u00dfnahmen (DQ, IQ, OQ, PQ)<\/li>\n\n\n\n<li>Durchf\u00fchrung von Messungen (Temperatur\/Druck\/Feuchte etc.) im Rahmen von Qualifizierungs- und Requalifizierungsma\u00dfnahmen<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>GMP \u2013 Services Kompetente Umsetzung von GMP-Anforderungen Der EU-GMP-Leitfaden (Good Manufacturing Practice) f\u00fcr Human- und Tierarzneimittel konfrontiert die Pharmabranche mit enormen Anforderungen. Diese zu erf\u00fcllen, ist ein Kraftakt in puncto Zeit und Ressourcen. \u00c4u\u00dferste Sorgfalt und fundiertes Fachwissen sind dabei Pflicht. Wir unterst\u00fctzen Sie professionell und kompetent bei der Umsetzung Ihrer GMP-Anforderungen, mit viel Liebe [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":2177,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","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":"disabled","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":"set","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":""},"class_list":["post-2226","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.3 - 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