Intelligent regulatory action for medical products

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In: IT/ICT, Medicine/medical devices, NMPA, Plan
29 May, NMPA (National Medical Products Administration) issued Intelligent regulatory action for medical products, integrating cloud computing, big data and Internet + information technology Construct Cloud Platform and Cloud Service for Medical Products Supervision Revise the informationization standards for medical products supervision, especially 20 informationization standards in five aspects: electronic license, drug traceability, drug category files, medical device coding database and cosmetics supervision Construct and manage medical products supervision data sharing platform, database, life cycle variety files for every product and every manufacturer Establish Information System for Drug, Medical Device and Cosmetics Supervision Establish drug traceability system, unique identification ofRead More →

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