| 英文摘要 |
Unlike general consumer products, medicinal products are closely associated with the health and lives of fellow citizens. Medicinal products are therefore subject to strict regulations and must acquire approved drug permit licenses from the central health authority before they may be sold on the market. TFDA is constantly reviewing and strengthening medicinal product monitoring systems to ensure drug use safety amongst the general public by revising pharmaceutical laws and harmonizing them with international standards, simplifying review processes and unifying management systems, monitoring the sources, distribution, and quality of drug manufacturing, prohibiting illegal drugs, and enforcing controlled drug management measures. |
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