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China Drug Registration

Meaning

China Drug Registration refers to the mandatory, multi-step regulatory process required for pharmaceutical companies to legally market and sell a drug within the People’s Republic of China. This stringent framework is overseen by the National Medical Products Administration (NMPA), formerly known as the China Food and Drug Administration (CFDA). The process ensures that all medicinal products meet the country’s high standards for safety, efficacy, and quality before they are made available to the public. Navigating this registration system is a critical, complex undertaking for both domestic and international drug manufacturers aiming to access the world’s second-largest pharmaceutical market.