The following quality management processes and applications can be used universally by any organization as a means to support QMS frameworks such as ISO 9000/9001, ISO 13485, IATF 16949 and others. They are generally applicable any function and can be used to drive operational excellence programs in Finance, Manufacturing, Supply Chain and even IT.
Per FDA, “the purpose of a Corrective Action and Preventive Action (CAPA) system is to collect information, analyze information, identify and investigate product, process and quality problems, and take appropriate and effective corrective and/or preventive action to prevent their recurrence.
Corrective Action and Preventive Action System is a core workflow available in KaizenKit that can be configured for use in many functional areas. Learn more about Corrective and Preventive Action System in KaizenKit.
Failure Reporting and Corrective Action System
Digital Standard Operating Procedures
Root Cause Analysis