Submit Comments to CMDE on “Requirements on Application Documents for Fast Track Evaluation of Medical Devices”

2016-05-31 | Beijing

The Centre of Medical Device Evaluation (CMDE) has issued a draft regulation how to accelerate evaluation for innovative medical devices for public consultation. The European Chamber submitted consolidated comments to the draft regulation, focussing on requirements to imported medical devices that may put importers on a disadvantegous position compared with locally manufactured products.

More information: http://www.cmde.org.cn/CL0002/4669.html