Abstract
Quality management in pharmaceutical industries is crucial as drugs are directly delivered to the customer’s body system, requiring identity, purity, and appropriate product quality. ICH Guidelines aim to ensure uniformity in products worldwide, aiding in export and import of drug products. Maintaining quality in products is complex and requires adherence to guidelines like GMP and GLP. Quality assurance departments in all pharmaceutical industries ensure compliance with these guidelines. Quality auditing checks internal and external aspects to ensure proper functioning. This paper focuses on the Quality management system in the Drug industry and its elements.
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