The Transformation of China's Drug Administration Law. China’s pharmaceutical regulatory landscape is undergoing a dramatic shift, with far-reaching implications for both domestic and international players.
Outline comprehensive regulations for drug research, registration, and market authorization, ensuring safety, efficacy, and quality control across TCM, chemical drugs, and biological products.
Provide a comprehensive framework for drug development, production, and distribution, emphasizing safety, efficacy, and accessibility while promoting innovation in both modern and TCM sectors.
