The General Office of the Jiangsu Provincial Government issued the “Notice on Certain Policies and Measures to Comprehensively Promote In-depth Pharmaceutical and Medical Device Supervision Reform to Promote the High-Quality Development of the Pharmaceutical Industry”. The “Notice” mentions that eligible group companies that have registered their products in the country will complete the technical review within 5 working days. Streamline product registration declaration materials in low-risk categories. The proposed listing registration of Class II medical devices is reviewed and approved in parallel with production license applications, and registration matters of continuation and change are handled together. The average test time limit for active medical devices was reduced from 85 working days to 60 working days.

The General Office of the Jiangsu Provincial Government issued the “Notice on Certain Policies and Measures to Comprehensively Promote In-depth Pharmaceutical and Medical Device Supervision Reform to Promote the High-Quality Development of the Pharmaceutical Industry”. The “Notice” mentions that eligible group companies that have registered their products in the country will complete the technical review within 5 working days. Streamline product registration declaration materials in low-risk categories. The proposed listing registration of Class II medical devices is reviewed and approved in parallel with production license applications, and registration matters of continuation and change are handled together. The average test time limit for active medical devices was reduced from 85 working days to 60 working days.