CAPA Management Software System - QualityzePosted by Qualityze on December 19th, 2022 Executing the process of root cause analysis is one of the crucial methods in identifying underlying issues, adopting the correct non-conformance actions and also ensures that they are avoided in the future. By taking this approach, it not only deals with the immediate issues but also allows you to identify them in the future before they become an issue. The flexibility of Qualityze CAPA management system helps and allows you to treat the most important part of a CAPA system, The Root Cause Analysis, in an efficient way by prioritizing the critical events and helping you make right decision – every time. It is suggested to get Qualityze CAPA Management Software solution today to treat nonconformance in a streamlined manner to avoid its reoccurrence. If you want to understand the product’s functionality and features completely then you can request a free demo or submit a technical support request on our contact page and our team will get back to you at the earliest. Qualityze CAPA Management software has an ability to works for all industries that includes Manufacturing, Life Sciences, Pharmaceuticals, Medical Devices, Nutraceuticals, Biologics, Food and Beverages, Automotive, Aerospace, and Defense Logistics, to assess risks and eliminate problems while maintaining compliance with applicable regulatory standards. Qualityze CAPA management software is designed in adherence with the industry standards and best practices which is defined by the regulatory authorities that includes Food and Drug Administration (FDA) – 21 CFR Part 820, International Organization for Standardization (ISO) – ISO 9001, ISO 13485 QMS software, Pharmaceuticals and Medical Devices Agency (PMDA), Therapeutic Goods Administration (TGA), China Food and Drug Administration (CFDA), etc.
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