CAPA PROCESS – STEP-BY-STEP INSTRUCTIONS (INFOGRAPHIC)

Corrective And Preventive Action (CAPA) is often discussed as it is an alarming issue for the life sciences industry. Organizations consider its importance and try to deal with it better as CAPA‘s are the key indicators of a process that investigates the problems, identifies the source, solves the issue with corrective actions, and prevents its reoccurrences by preventive measures.  Any flaws in the process would lead to FDA (Food and Drug Administration)  warning letters and compliance grievances.  

So, iQuality has produced a step-by-step process to help companies handle the CAPA process to get satisfactory results in adherence to ISO (International Standards Organization) FDA regulations.  

Every problem cannot be a CAPA and cannot ignore a minor NC (Non-Conformance), leading to a systematic issue. QMS (Quality Management System) will make you define, manage, and implement an effective CAPA process meeting the regulation requirements for a quality management system. A proper and effective CAPA process is proof of an effective quality system of an organization and speaks about the safety and quality measures followed by the production staff. 

For more information about CAPA PROCESS STEPS visit our website: Read More.



 

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