《互联网药品医疗器械信息服务备案管理规定》发布

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] Summary by Relevant Categories Regulations - The new regulations clarify the content, conditions, procedures, and required materials for the filing of internet drug and medical device information services [1] - The implementation of these regulations aims to further standardize the management of internet drug and medical device information service filings [1] Industry Impact - The regulations are expected to effectively guide local authorities in the standardized execution of filing work [1]