With the continuous development and maturity of China's socialist market economic system and changes in the international economic environment, China's pharmaceutical industry is facing new opportunities, difficulties and challenges while achieving further development. In this context, drug development and drug evaluation are facing new challenges such as innovation, intellectual property rights, improved quality of imitation filings, and technical requirements related to this.
In order to promote the common development of drug research and development and technical review, the Drug Evaluation Center of the State Food and Drug Administration will hold a seminar in Beijing on October 20-21 to analyze the situation and current situation of China's independent drug innovation and explore innovative drug development. The third session of the Drug Technology Review Symposium on the theme of Evaluation Strategies. The conference will invite experts and scholars at home and abroad to conduct drug research and development, production and drug evaluation, and the heads of large enterprises and relevant government officials to discuss the topic.
The third seminar on drug technology review will be held in the form of the main conference venue and three special sessions. The theme of the main venue is “Exploring strategies for innovative drug development and evaluation in the historical transition from imitation to innovationâ€. The topics of the three sub-meetings are: “Research and exploration of the evaluation method of Chinese medicine effectivenessâ€; “Quality control and technical requirements for the development of chemical products in national standards, and evaluation of the rationality of dosage forms in drug research and developmentâ€; Research and exploration of clinical and clinical safety and effectiveness."
The seminar will also invite relevant leaders of the Ministry of Science and Technology, the State Food and Drug Administration, and nearly 30 experts and scholars engaged in drug review, drug research and development and registration management at home and abroad to conduct special reports and discussions on relevant topics.
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