First and foremost, CAPA is a mandatory requirement for manufacturers of medical devices. Therefore, it is essential for compliance.
Second, corrective action helps to identify the root cause and improve the quality of processes to ensure the quality of the product/service.
Third, It helps with the continuous improvement of the quality management system.
Fourth, it enables a ... https://www.compliancequest.com/bloglet/corrective-vs-preventive-action/