15
2023
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05
Medical device production supervision platform cross-regional commissioned production inspection and other new functions of the online training will be successfully held
In order to implement the newly revised Regulations on the Supervision and Administration of Medical Devices and the Measures for the Supervision and Administration of Medical Device Production, combined with the relevant standards and norms of the "Internet + Supervision" of The State Council, the Information Center has optimized and upgraded the medical device production supervision platform, and designed and developed new functions such as cross-regional commissioned production inspection. According to the needs of the work, the information Center cooperated with the device supervision Department to hold an online training meeting on the introduction of related new functions on the morning of September 16. The information center carefully designs the training content and strives to enhance the guidance and practicability of the training. At the training meeting, the information center introduced the background and construction needs of the new function construction, and demonstrated in detail the annual self-inspection report of the medical device manufacturer, the production product report, the production shutdown report, the production condition change report, and the functional operation process of cross-regional commissioned production report, inspection, and information sharing. Nearly 150 people from relevant departments and bureaus of the bureau and provincial drug administration 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 better meet the needs of medical device production and supervision business. (Wang Yanbo)
Source: Suzhi Drug Administration
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