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To further advance the implementation of the vaccine regulatory quality management system and promote the coordination of quality management systems within the pharmaceutical regulatory system, thereby enhancing the operation level of quality management system construction, the National Medical Products Administration held regional exchange meetings on the construction of China's vaccine regulatory quality management system in Nanjing on May 16 and in Urumqi on May 30.
The meeting reported on the construction and operation of the National Medical Products Administration's (NMPA) vaccine regulatory quality management system, and introduced the experiences in quality management practices such as the internal control system of the NMPA, vaccine registration and marketing authorization quality management, internal audits, and service recipient satisfaction surveys. The National Institutes for Food and Drug Control (NIFDC), the Inspection Center, and the Center for Medical Device Evaluation respectively presented on the consistent development of the vaccine lot-release network laboratories, the construction of drug inspection quality management systems, and the operation of medical device technical evaluation quality management systems. The Jiangsu Provincial and Xinjiang Uygur Autonomous Region Medical Products Administration bureaus exchanged information on the operation of their provincial-level vaccine regulatory quality management systems. Participating local pharmaceutical regulatory departments discussed and shared experiences on the construction, operation, and advancement of quality management systems based on their respective provincial conditions, offering suggestions and opinions to strengthen system building.
Officials from relevant departments of the National Medical Products Administration (NMPA), as well as division-level cadres responsible for quality management from provinces (regions, municipalities) and the Xinjiang Production and Construction Corps, attended the meeting in regional groups.




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