国家药品和医疗器械审评检查京津冀分中心在北京挂牌运行

Core Viewpoint - The establishment of the Beijing-Tianjin-Hebei (Jing-Jin-Ji) Center for Drug and Medical Device Review and Inspection is a significant step by the National Medical Products Administration (NMPA) to enhance the drug and medical device approval system, promote innovation, and support high-quality development of the regional pharmaceutical industry [1][2] Group 1: Center Functions and Responsibilities - The Jing-Jin-Ji Center will serve the regions of Beijing, Tianjin, Hebei, and Shandong, providing technical services related to drug and medical device review, including research guidance, consultation acceptance, and review communication [1] - The center will also undertake registration verification and conduct inspections, contributing to the overall efficiency and quality of the review process [2] Group 2: Regional Pharmaceutical Industry Impact - Since 2021, the Jing-Jin-Ji region has approved 34 innovative drugs, accounting for 16.2% of the national total, and 68 Class III innovative medical devices, representing 25.7% of the national total [1] - The pharmaceutical industry's revenue in the region is projected to reach 841.5 billion yuan in 2024, which will constitute 28.3% of the national revenue [1]