Circular of the General Administration of the people's Republic of China on Soliciting Opinions on the measures for the administration of medical device standards (Draft for comments)

Source: CFDA 2016-11-1 in order to strengthen the management of medical device standards and ensure the safety and effectiveness of medical devices, in accordance with the standardization law of the people's Republic of China and the regulations on the supervision and administration of medical devices, the State Food and drug administration has implemented the current measures for the management of medical device standards (Trial) (Order No 31 of the original administration) No.) has been revised to form the "management measures for medical device standards" (Draft for comments), and now it is open to the public for comments Before November 30, 2016, all sectors of the society can log in to the legal information network of the Chinese government (website: http://www.chinalaw.gov.cn) and enter the "opinion collection system for draft regulations and rules" on the left side of the home page to make comments and suggestions.