Seminar on Evaluation and Approval of Medical Devices

2015-11-30 | Beijing

WLM presented the updates of Order 650 implementation regulations. LZ’s presentation was on the overall work of CMDE. Officials from Japan introduced the state of art of medical device supervision in Japan. The meeting was hold very formally, with little discussion in details. During the panel discussion, one of the key concerns of industry, which is the possibility of pre-consultation with CMDE for new product submissions, was asked to LZ. The answer is at current stage, it should be processed through CMDE regular open-day for consultation. JY on behalf of the Chamber, was invited and introduced as one of the VIPs for the meeting.

More information: http://www.sfda.gov.cn/WS01/CL0001/