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Recently, Lei Ping, a member of the party group and deputy director of the State Drug Administration, went to Guangdong and Yunnan to attend medical device registration management work area symposiums, and visited the South China University of Technology Regulatory Research Center, Guangzhou Laboratory, Yunnan Fuwai Cardiovascular Hospital, and innovative medical device companies to learn more about medical device registration management and innovative research and development. At the meeting, Lei Ping fully affirmed the medical device registration management work in 2025, and emphasized the need to carefully study and implement the spirit of the Fourth Plenary Session of the 20th CPC Central Committee, thoroughly analyze the opportunities and challenges facing medical device registration management on the basis of a comprehensive summary of the “14th Five-Year Plan” work, adhere to people's health needs, coordinate high-quality medical device development and safety, and plan the “15th Five-Year Plan” development initiatives and goals from a high starting point.

Zhitongcaijing·12/15/2025 03:49:04
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Recently, Lei Ping, a member of the party group and deputy director of the State Drug Administration, went to Guangdong and Yunnan to attend medical device registration management work area symposiums, and visited the South China University of Technology Regulatory Research Center, Guangzhou Laboratory, Yunnan Fuwai Cardiovascular Hospital, and innovative medical device companies to learn more about medical device registration management and innovative research and development. At the meeting, Lei Ping fully affirmed the medical device registration management work in 2025, and emphasized the need to carefully study and implement the spirit of the Fourth Plenary Session of the 20th CPC Central Committee, thoroughly analyze the opportunities and challenges facing medical device registration management on the basis of a comprehensive summary of the “14th Five-Year Plan” work, adhere to people's health needs, coordinate high-quality medical device development and safety, and plan the “15th Five-Year Plan” development initiatives and goals from a high starting point.