{"id":2537,"date":"2020-05-16T09:44:46","date_gmt":"2020-05-16T07:44:46","guid":{"rendered":"https:\/\/q-finity.de\/?post_type=encyclopedia&#038;p=2537"},"modified":"2023-07-12T13:59:19","modified_gmt":"2023-07-12T11:59:19","slug":"computerized-system-validation","status":"publish","type":"encyclopedia","link":"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/","title":{"rendered":"Computerized System Validation"},"content":{"rendered":"<p><a href=\"https:\/\/q-finity.de\/en\/glossar\/computerized-system\/\" target=\"_self\" title=\"A Computerized System is a broad range of systems including, but not limited to, automated laboratory equipment, laboratory information management, clinical trials data management, vigilance systems, process control and process analytics, manufacturing resource planning, automated manufacturing equipment, manufacturing execution, and document management systems. The computerized system consists of the hardware, software, and network components, together&hellip;\" class=\"encyclopedia\">Computerized system<\/a> validation describes achieving and maintaining compliance with applicable GxP and Medical Device regulations and establishing documented evidence that the system is fit for intended use by:<\/p>\n<ul>\n<li>the adoption of principles, approaches, and life cycle activities within the validation framework by executing project specific validation plans<\/li>\n<li>establishing and applying&nbsp;appropriate operational controls throughout the life of the system<\/li>\n<\/ul>\n<p>If you need more information about <a href=\"https:\/\/q-finity.de\/en\/glossar\/computerized-system\/\" target=\"_self\" title=\"A Computerized System is a broad range of systems including, but not limited to, automated laboratory equipment, laboratory information management, clinical trials data management, vigilance systems, process control and process analytics, manufacturing resource planning, automated manufacturing equipment, manufacturing execution, and document management systems. The computerized system consists of the hardware, software, and network components, together&hellip;\" class=\"encyclopedia\">computerized system<\/a> validation please contact us <a href=\"https:\/\/q-finity.de\/en\/contact\/?swcfpc=1\">here<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Computerized system validation describes achieving and maintaining compliance with applicable GxP and Medical Device regulations and establishing documented evidence that the system is fit for intended use by: the adoption of principles, approaches, and life cycle activities within the validation framework by executing project specific validation plans establishing and applying\u00a0appropriate operational controls throughout the life [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"template":"","encyclopedia-tag":[],"class_list":["post-2537","encyclopedia","type-encyclopedia","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v26.8 (Yoast SEO v26.8) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Computerized System Validation Glossary<\/title>\n<meta name=\"description\" content=\"Computerized System Validation describes compliance with applicable GxP and Medical Device regulations and establishing documented evidence.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Computerized System Validation\" \/>\n<meta property=\"og:description\" content=\"Computerized System Validation describes compliance with applicable GxP and Medical Device regulations and establishing documented evidence.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/\" \/>\n<meta property=\"og:site_name\" content=\"QFINITY\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/QFINITY\" \/>\n<meta property=\"article:modified_time\" content=\"2023-07-12T11:59:19+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:site\" content=\"@cQFINITY\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/\",\"url\":\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/\",\"name\":\"Computerized System Validation Glossary\",\"isPartOf\":{\"@id\":\"https:\/\/q-finity.de\/en\/#website\"},\"datePublished\":\"2020-05-16T07:44:46+00:00\",\"dateModified\":\"2023-07-12T11:59:19+00:00\",\"description\":\"Computerized System Validation describes compliance with applicable GxP and Medical Device regulations and establishing documented evidence.\",\"breadcrumb\":{\"@id\":\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Startseite\",\"item\":\"https:\/\/q-finity.de\/en\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Glossar\",\"item\":\"https:\/\/q-finity.de\/en\/glossar\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Computerized System Validation\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/q-finity.de\/en\/#website\",\"url\":\"https:\/\/q-finity.de\/en\/\",\"name\":\"QFINITY\",\"description\":\"Qualit\u00e4tsmanagement &amp; 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