国家药监局副局长雷平在浙江调研医疗器械注册管理和创新研发工作

Core Viewpoint - The National Medical Products Administration (NMPA) emphasizes the need to enhance the registration and management of medical devices, focusing on clinical demand and innovation transformation [1] Group 1: Regulatory Focus - The NMPA aims to leverage regional advantages to improve the level of registration and filing work for medical devices [1] - There is a call for a supportive system and mechanism for medical device innovation [1] Group 2: Innovation and Collaboration - The NMPA stresses the importance of strengthening the linkage between research and review processes [1] - Promoting the integration of medical and engineering fields is highlighted as essential for fostering an innovative development ecosystem [1] Group 3: Clinical Value - The goal is to facilitate the transformation of research outcomes with significant clinical value into medical device products [1]