CAPA Management Software

CAPA system is a concept within good manufacturing practice GMP and numerous ISO business standards. This focus on the systematic investigation of the root causes of the identified issues or identified risks in an attempt to prevent their recurrence for corrective action or to prevent occurrence for preventive action. Qualityze CAPA management software makes a deep investigation into quality issues to obligate the root cause and prevents recurrence by using its intuitive and configurable workflows, fields, dashboards and reports.    

This software is developed in adherence with industry standards and best practices defined by the regulatory authorities including the 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.