{"id":14164,"date":"2025-08-02T15:05:40","date_gmt":"2025-08-02T13:05:40","guid":{"rendered":"https:\/\/q-finity.de\/?p=14164"},"modified":"2026-07-19T09:00:07","modified_gmt":"2026-07-19T07:00:07","slug":"29th-gqma","status":"publish","type":"post","link":"https:\/\/q-finity.de\/en\/29th-gqma\/","title":{"rendered":"29th GQMA Annual Conference with QFINITY | September 18-19, 2025"},"content":{"rendered":"<p data-start=\"134\" data-end=\"291\">We are pleased to be part of the 29th Annual Conference of the GQMA (Society for <a href=\"https:\/\/q-finity.de\/en\/glossar\/quality-management\/\" target=\"_self\" title=\"Quality Management (QM) refers to all organizational measures that relate to the structure of the organization and the efficient execution of processes at various levels of the company. With consistent implementation, quality management enables the continuous improvement of corporate culture, process quality and technology deployment, ultimately leading to better products or services.\" class=\"encyclopedia\">Quality Management<\/a> in the Pharmaceutical Industry) once again this year!<\/p>\n<p data-start=\"293\" data-end=\"396\">The event will take place on September 18-19, 2025, at the Steigenberger Hotel in Bad Neuenahr.<\/p>\n<p data-start=\"398\" data-end=\"602\">Senior Executive Consultant Frank Henrichmann will give a presentation titled:<br data-start=\"480\" data-end=\"483\">&ldquo;Future-Proof QA Strategies for <a href=\"https:\/\/q-finity.de\/en\/glossar\/computerized-system-validation\/\" target=\"_self\" title=\"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&nbsp;appropriate operational controls throughout the life&hellip;\" class=\"encyclopedia\">Computerized System Validation<\/a>: From Documentation Overload to Control Objectives.&rdquo;<\/p>\n<p data-start=\"604\" data-end=\"1101\">The talk addresses key challenges currently facing quality assurance in IT validation projects. It focuses on the shift away from rigid, document-heavy processes toward flexible, risk-based, and system-oriented QA approaches. Frank Henrichmann will provide practical insights into how QA departments can contribute to <a href=\"https:\/\/q-finity.de\/en\/glossar\/computerized-system\/\" target=\"_self\" title=\"The term computerized system covers 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,&hellip;\" class=\"encyclopedia\">Computerized System<\/a> Validation (CSV) in an efficient and value-adding way &ndash; with less administrative burden and more focus on what truly matters: Control Objectives.<\/p>\n<p data-start=\"1103\" data-end=\"1133\">Key discussion points include:<\/p>\n<ul data-start=\"1134\" data-end=\"1421\">\n<li data-start=\"1134\" data-end=\"1208\">\n<p data-start=\"1136\" data-end=\"1208\">What competencies are essential for QA in modern IT validation projects?<\/p>\n<\/li>\n<li data-start=\"1209\" data-end=\"1264\">\n<p data-start=\"1211\" data-end=\"1264\">Does the document-based approach still have a future?<\/p>\n<\/li>\n<li data-start=\"1265\" data-end=\"1348\">\n<p data-start=\"1267\" data-end=\"1348\">How can QA create real value through critical thinking and risk-based evaluation?<\/p>\n<\/li>\n<li data-start=\"1349\" data-end=\"1421\">\n<p data-start=\"1351\" data-end=\"1421\">How much standardization is helpful &ndash; and when does it become a barrier?<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"1423\" data-end=\"1496\">Join our session and meet us on site &ndash; we look forward to talking with you!<\/p>\n<p data-start=\"1498\" data-end=\"1627\">You can find more information about the 29th GQMA Annual Conference <a href=\"https:\/\/www.gqma.de\">here<\/a>. For additional events with QFINITY, click <a href=\"https:\/\/q-finity.de\/en\/meet-qfinity\/\">here<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>We are pleased to be part of the 29th Annual Conference of the GQMA (Society for Quality Management in the Pharmaceutical Industry) once again this year! The event will take place on September 18-19, 2025, at the Steigenberger Hotel in Bad Neuenahr. Senior Executive Consultant Frank Henrichmann will give a presentation titled:\u201cFuture-Proof QA Strategies for [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":14131,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false,"footnotes":""},"categories":[38],"tags":[],"class_list":["post-14164","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-meet-qfinity-en"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v28.0 (Yoast SEO v28.1) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>29th GQMA Annual Conference: CSV Strategy Talk | QFINITY<\/title>\n<meta name=\"description\" content=\"QFINITY at the 29th GQMA Annual Conference (18.-19.09.2025, Bad Neuenahr): Frank Henrichmann spoke on QA strategies for computer system validation.\" \/>\n<meta name=\"robots\" content=\"index, follow, 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