Question
What do you understand by 'Adulteration of Drugs'? Briefly discuss types of deliberate adulteration.
Answer :
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Adulteration of drugs refers to the practice of reducing the quality, safety, and efficacy of pharmaceutical products by mixing or substituting them with inferior, cheap, or harmful substances. In the context of management, adulteration of drugs is considered a serious issue because it not only affects the health of consumers but also damages the trust, reputation, and sustainability of healthcare and pharmaceutical organizations. It is an unethical and illegal practice that violates quality control standards, regulatory norms, and professional ethics. Managers in the pharmaceutical sector must therefore ensure that raw materials, manufacturing processes, and distribution systems are closely monitored to prevent adulteration and to maintain the integrity of products. Adulteration
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