involving 5 fields including automobiles and medicine! beijing releases negative list to facilitate cross-border data flow
2024-08-31
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this article is transferred from [cctv news client];
on august 30, beijing issued the "china (beijing) pilot free trade zone data outbound management list (negative list) (2024 edition)", which further clarified the scope of data that needs to be included in the outbound management, and moderately relaxed the conditions for declaring personal information outbound. data outside the negative list can flow freely across borders.
cross-border data flow is the basis for the exchange and sharing of global capital, information, technology and other resource elements. the first batch of the negative list involves five fields: automobile, medicine, retail, civil aviation and artificial intelligence.
hong yanqing, professor of law school of beijing institute of technology:the export of important data needs to go through national cybersecurity management measures. the business community generally reflects that it is relatively difficult to identify what is important data. beijing's negative list has made this clearer, so companies can clearly check the list. data outside the negative list can flow freely, which obviously provides great convenience for companies' cross-border operations, cross-border joint research and cross-border marketing.
also released at the same time as the negative list were the "china (beijing) pilot free trade zone data outbound negative list management measures (trial)" and the "beijing data cross-border flow facilitation service management measures", which further optimized the data outbound compliance declaration method, simplified the filing process, and launched the beijing data cross-border facilitation information service platform to better serve the cross-border data flow needs of enterprises.
yang hu, director of the cybersecurity coordination division of beijing internet information office:on the basis of ensuring that risks are manageable and controllable, taking the drug clinical trial scenario as an example, previously when the personal information of more than 10,000 people went abroad, a security assessment was required. we have raised this standard by 50,000 people, which will allow most drug research and development companies to transform from prior assessment to filing, greatly simplifying the procedure.
