Corrective Action / Preventive Action (CAPA)

The implementation of a Corrective Action / Preventive Action (CAPA) is a required quality measure that must be maintained in order to comply with governmental regulation.

The critical and dynamic nature of CAPA processes require the highest levels of accuracy, methodology and, most importantly, flexibility. Rigorous regulatory and traceability requirements exist in industries such as aerospace, automotive, defense, life sciences or any other manufacturing operation. Integrating corrective action / preventive action CAPA system processes enterprise-wide has always been an important part of any corporate quality system, regardless of the industry. Even if a company is not registered ISO 9000, ISO 8402 or under FDA requirements, it is a good business practice to have systems in place to correct recurring problems and to prevent new problems from occurring.

FavoWeb CAPA collects and gathers in one database customer complaints, non-conformances, corrective/ preventive actions that were implemented in the past and any other safety related data.  

Using FavoWeb FRACAS, CAPA can help your company to continually carry out improvements within your organization. FavoWeb CAPA is a closed loop process starting from the problem itself and ending in the implementation of the corrective action/ preventive action that should be taken. Each one of these actions is a result of a sophisticated and full analysis, based on FavoWeb vast experience.