Qualityze EQMS for CAPA Management Software

 


An advanced CAPA management system offers closed-loop issues resolution and also enables a manufacturer to identify, analyze and also share crucial product quality data across the enterprise. Qualityze CAPA management software provides a secure, centralized repository for all sorts of CAPA documents. The flexibility feature of this Qualityze CAPA management software system allows you to document the multiple actions plans to address the root cause which are identified during the investigation task. This software also provides the multiple investigation tools, including five whys. CAPA management software system of Qualityze allows users to create and track workflows and other documentation with extensive flexibility in defining every step in CAPA. 

CAPA management software of Qualityze is been designed in adherence with the industry standards and best practices that 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.  

CAPA management software of Qualityze 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.  

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