国家药监局发布新规 进一步规范互联网药品医疗器械信息服务备案管理

Core Viewpoint - The National Medical Products Administration (NMPA) has issued the "Regulations on the Filing Management of Internet Drug and Medical Device Information Services," which will take effect immediately upon publication [1] Group 1: Regulatory Framework - The regulations are an important measure by the NMPA to implement the State Council's reform spirit of "separation of licenses and permits" [1] - The regulations require that internet drug and medical device information services must file with the provincial drug supervision management department according to the specified requirements [1] Group 2: Filing Management - The regulations clarify the content, conditions, procedures, and required materials for the filing of internet drug and medical device information services [1] - The introduction of these regulations will further standardize the filing management of internet drug and medical device information services and effectively guide localities in conducting filing work [1]