Attention! In 2019, 94 plans for the formulation and revision of medical device industry standards have been determined

In accordance with the requirements of the measures for the administration of medical device standards and the code for the administration of the preparation and revision of medical device standards, the State Drug Administration has organized the selection of the preparation and revision of medical device industry standards in 2019 After public consultation and expert argumentation, 94 items of the preparation and revision of medical device industry standards in 2019 have been determined, which are now publicized During the publicity period, if you have any objection to the planned project, please give feedback to SDA Publicity time: December 11-17, 2018 contact person and Tel: Huang lunliang, 010-88331421 address: Department of device registration, State Drug Administration, building 2, No 26, Xuanwumen West Street, Xicheng District, Beijing Post Code: 100053 annex of general department, State Drug Administration, December 10, 2018, 2019 medical device industry standard development and revision plan project (click the picture to see the big picture)