CONTROL OF NON-CONFORMANCE OF PRODUCTS AND PROCEDURE

Description

Control of non-conformances is a critical aspect of quality management in the pharmaceutical industry. When non-conformances, such as deviations from specifications or procedures, are identified, a rigorous process is initiated to investigate the root cause, contain the issue, and implement corrective and preventive actions (CAPAs). This involves documenting the non-conformance, assessing its impact, and determining appropriate corrective actions. Once corrective actions are implemented, verification activities are conducted to ensure effectiveness. By effectively managing non-conformances, pharmaceutical companies can maintain product quality, prevent recurrence of issues, and comply with regulatory requirements.