December 22, 2025 - The National Medical Products Administration (NMPA) has announced the "Provisions on the Administration of Filing for 

Online Drug and Medical Device Information Services," which took effect immediately upon release.

As a key measure to advance the "separation of permits and licenses" reform, the new Provisions clarify filing procedures, requirements, and 

necessary documentation. Entities providing such information services must now file a record with the provincial-level medical products 

administration where they are located.

This regulation is expected to standardize the filing process nationwide, enhance oversight, and foster the sector's healthy development.