On November 18, 2020, the 11th China International Conference on the supervision and management of medical devices (cimdr), sponsored by China food and drug International Exchange Center (ccfdie), opened in Fuzhou Strait International Convention and Exhibition Center, Fujian Province. Relevant leaders from the State Drug Administration and Fujian Province attended and addressed the opening ceremony.
The meeting closely combined with the current focus of medical device supervision and anti epidemic hot spot, focusing on the theme of "improving, innovating, contributing Chinese wisdom to global regulation", the relevant responsible persons of the medical device registration and management department, the medical device supervision department, the device Audit Center, the standard management center, and the evaluation center of the State Drug Administration comprehensively analyzed and detailed the regulatory regulations of medical devices in China This paper introduces the reform of medical device review and approval system, standard management, adverse event monitoring, traceability system construction, industrial development, international cooperation and other aspects. Medical device regulatory authorities and industry experts from the United States, Japan, Saudi Arabia and other countries and regions shared the relevant national and regional medical device regulations and regulatory new measures, new development and new harvest through online and offline, and discussed how the medical device field should cope with the epidemic challenge in the global anti epidemic environment.
In addition to the plenary session, the meeting also focused on the hot issues in the current medical device industry, and set up 16 sub venues, including medical device innovation technology and product branch, medical device clinical evaluation branch, medical device regulatory science and real world data (RWE) branch, emergency management and epidemic prevention and protection products branch (including body temperature management topic), research and development and application of domestic medical devices 。 Experts and scholars in the medical device industry at home and abroad communicated and exchanged around the latest topics and cutting-edge technologies of medical devices.
Two parallel meetings were held at the same time, which promoted the medical device regulatory industry. The parallel meeting of "medical device managers Conference (MD50)" was attended by the industry leaders of the most innovative and influential medical device enterprises, investment institutions and regulatory departments in the world, and jointly discussed the new opportunities for industrial development; the parallel meeting of "regulatory affairs talent development" jointly discussed the new way of talent development in the industry with relevant training institutions, colleges and universities, regulatory authorities, etc Law.