Core Viewpoint - The National Medical Products Administration (NMPA) emphasizes the importance of enhancing the quality and safety supervision of medical devices while promoting innovation in the industry [1] Group 1: Industry Development - The NMPA acknowledges the recent development of the medical device industry in Chongqing and the effectiveness of quality safety supervision [1] - There is a call for a more robust quality safety responsibility system for medical devices, focusing on the entire product lifecycle [1] Group 2: Regulatory Framework - The NMPA stresses the need to strengthen regulatory mechanisms to ensure safety standards are upheld [1] - The agency aims to support the development of innovative medical devices to foster high-quality industrial growth [1]