Comments on “Guiding Principles for Registration and Technical Evaluation of Central Venous Catheters“

2016-11-11 | Beijing

The Healthcare Equipment Working Group submitted Comments on the draft “Guiding Principles for Registration and Technical Evaluation of Central Venous Catheters“ to the Centre of Medical Device Evaluation (CMDE) of the CFDA.

The recommendations focused on the documents required for registration and details how clinical trials must be designed.

More information: http://www.cmde.org.cn/CL0004/5429.html