From October 14 to 15, Lei Ping, member of the party group and deputy director of the State Drug Administration, attended a special training course on medical device standard innovation and high-quality development in Shijiazhuang and delivered a speech. Lei Ping fully acknowledged the achievements made in medical device standardization, stressing the need to earnestly implement the decisions and arrangements of the Party Central Committee and the State Council to deeply grasp the significance of medical device standards work; implement a new round of standard improvement action plans, promote pre-standardization research in cutting-edge key areas, further strengthen the leading and supporting role of standards; raise the level of internationalization of standards with more practical measures to help Chinese medical device products go global through standard connectivity. The heads of the Device Registration Department and the Device Standard Control Center introduced key work progress and follow-up measures. Nine provincial drug administration heads, provincial medical device inspection agencies, and chairman members of various standard committees participated in the training. Lei Ping also conducted field research on medical transformation and innovative research and development in medical institutions and medical device companies.

From October 14 to 15, Lei Ping, member of the party group and deputy director of the State Drug Administration, attended a special training course on medical device standard innovation and high-quality development in Shijiazhuang and delivered a speech. Lei Ping fully acknowledged the achievements made in medical device standardization, stressing the need to earnestly implement the decisions and arrangements of the Party Central Committee and the State Council to deeply grasp the significance of medical device standards work; implement a new round of standard improvement action plans, promote pre-standardization research in cutting-edge key areas, further strengthen the leading and supporting role of standards; raise the level of internationalization of standards with more practical measures to help Chinese medical device products go global through standard connectivity. The heads of the Device Registration Department and the Device Standard Control Center introduced key work progress and follow-up measures. Nine provincial drug administration heads, provincial medical device inspection agencies, and chairman members of various standard committees participated in the training. Lei Ping also conducted field research on medical transformation and innovative research and development in medical institutions and medical device companies.