In order to implement the newly revised "Regulations on the Supervision and Administration of Medical Devices" and "Measures for the Supervision and Administration of Medical Device Production", combined with the relevant standards and specifications of the State Council's "Internet Supervision", the Information Center has optimized and upgraded the medical device production supervision platform, and designed and developed cross-regional commissioned New functions such as production inspection. According to the needs of the work, the Information Center, in cooperation with the Equipment Supervision Department, held an online training meeting on the morning of September 16 to introduce relevant new functions. The information center carefully designed the training content, and strive to enhance the training guidance and practicality. At the training meeting, the information center introduced the construction background and construction requirements of new functions, and demonstrated in detail the annual self-examination report, production product report, production shutdown report, production condition change report of medical device manufacturers, as well as cross-regional entrusted production report, inspection, information sharing and other functional operation processes. Nearly 150 people from relevant departments and bureaus of the bureau and provincial drug administrations participated in the training online. In the next step, the information center will continue to optimize and improve the functions of the regulatory platform system to meet the needs of medical device production supervision business.