On 25th June, the ministry of justice published the amended regulation on supervision and management of medical devices (draft) and called for public comments. Deadline was 24th July 2018. The main amended contents were listed as follow:

            Consummate the marketing authorization holder of medical devices

            Reform the management of clinical trials

            Consummate the approval process

            Consummate the market surveillance

http://www.moj.gov.cn/government_public/content/2018-06/25/tzwj_21121.html