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 process of intentionally or unintentionally lowering the quality, purity, or strength of pharmaceutical products by mixing them with inferior, harmful, or non-permissible substances. It is a serious issue in the field of healthcare and pharmaceuticals as it not only reduces the effectiveness of medicines but can also endanger the lives of patients. In the context of management, adulteration is seen as an unethical and unlawful practice that violates regulatory standards, damages organizational reputation, and reduces consumer trust. Managers in pharmaceutical industries are therefore required to ensure strict quality control, compliance with legal frameworks, and implementation of good manufacturing practices to avoid such practices. Adulteration not only leads to health hazards but also disrupts the entire supply chain and invites legal
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