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Adulteration of drugs refers to the act of intentionally or unintentionally adding impurities, foreign substances, or inferior quality materials to medicinal products, thereby reducing their quality, safety, and efficacy. It is a significant concern in the pharmaceutical industry as it can pose serious health risks to consumers and compromise the trust in medical treatments. Adulteration can occur at any stage of drug production, including manufacturing, packaging, storage, and distribution. From the perspective of management, preventing adulteration involves implementing strict quality control measures, regulatory _____ _________ _________ ___ ________ ____ ____ _____ ______.
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