A Quality Management System (QMS) in pharmaceutical manufacturing is a comprehensive framework designed to manage quality through structured policies, processes, and procedures. It aims at ensuring consistent product quality, customer satisfaction, regulatory adherence, and ongoing improvement. The system integrates quality planning, control, assurance, risk management, documentation, corrective and preventive actions, and management reviews, emphasizing a formalized approach to maintain quality across all manufacturing stages, from planning through to continuous improvement efforts. This holistic view supports the organisation’s quality objectives and operational excellence.
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