CAPA management process is a quality management methodology which allows for formal documentation and also assessment of the industry and business issues. By this CAPA management software of Qualityze, you can easily document the quality issues, potential risks and then also decide on the action plan after complete analysis. Furthermore, the issue identified must be a valid nonconformance for risk assessment and an action plan to be implemented for the same.
Qualityze Corrective Action preventive Action 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.
Qualityze CAPA management software enables you to capture all the CAPA related information through its user-friendly forms. This includes Title, Description, Problem Statement, CAPA Source, and Auto-generated Number, Reported Date, Reported By, Criticality, CAPA Owner, and much more.
Qualityze is CAPA system cloud-based platform which focus on all IT disciplines without you necessary having to be an expert in them all. This automated CAPA management system reduces audit time and findings and also decreases the risk of product recalls. This software improves product quality and safety and also increases customer satisfaction and ensures regulatory compliance.