CAPA program is a method to address and correct problems in the workplace before they cause further damage. Qualityze CAPA Management Software eliminates systematic issue like deviations, nonconformances, defects and others by identifying their root causes by successful investigation and makes sure that it won't occur later. From this Qualityze CAPA Management Software, you can easily perform the following activities like CAPA Initiation, Investigation, Root cause analysis, Risk assessment, Planning & Implement Action Plans, Effectiveness Review, Resolution Activities, Verification, Digital Signature Validation.
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.