State Drug Administration Seeks Public Feedback on Draft Measures to Streamline Regulation and Boost Innovation in High-End Medical Devices

2025-03-31 / Read about 0 minute

Author：小编

The General Office of the State Drug Administration invites the public to comment on the 'Draft Measures to Optimize Full Lifecycle Regulation and Support Innovation and Development of High-End Medical Devices'. The draft aims to expedite the revision and development of standards for cutting-edge sectors, including medical robots, AI-integrated medical devices, and advanced medical imaging equipment, while also establishing pertinent standardization technical committees. Furthermore, it emphasizes strengthening research into the standardization of novel biomaterials, encompassing additive manufacturing medical materials, flexible electrodes for brain-computer interfaces, and synthetic biomaterials derived from genetic engineering.

Previous page："China Ranks 10th in Comprehensive Innovation Capa...

Next page：AI Programming Boom: Over 1600 Participants in 30 ...

Return to List

Hot Reading

2 day ago

Nalini Priya Uppari Established AI DOC Co-pilot at Enterprise Innovation with AI for Governance and Compliance as Her Organization's Core Business Focus

2 day ago

Sustaining AI Performance: Engineering Reliable GPU Systems

2 day ago

Evidence Grows That GPT-5 Is a Bit of a Dud

1 day ago

This new Gemini AI feature could make your life so much more efficient