Use this "List of CAPAs" template to efficiently track and document all implemented Corrective and Preventive Actions within your quality management system, supporting compliance with ISO 13485, EU MDR, and FDA 21 CFR 820 requirements. You should maintain and update this list whenever a new CAPA is initiated or completed to ensure transparent oversight and facilitate audits or inspections. This tool helps you demonstrate ongoing quality improvement and effective issue resolution in your medical device processes.