CAPA Management Software System - Qualityze

 Generally, CAPA is considered as the stand-alone process which is managed in point solution. Sometimes you might not even know the data value when it comes to CAPA management system until you begin to close the loop on quality. In dependence of the particular manufacturing segment, automating CAPA with the quality management software system enables synergies across the enterprise by offering visibility into supplier management issues. Qualityze CAPA management software comes with the feature-packed solution with a user-friendly interface to handle CAPA with complete convenience and efficiency. By this software, you can document the quality issues, their potential risks, and decide on the action plan after complete analysis. However, the issue identified must be a valid nonconformance for risk assessment and an action plan to be implemented for the same.

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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