To further unify the understanding of mandatory industry standards, and truly promote the implementation of mandatory industry standards of medical devices, in accordance with the Standardization Law of the People's Republic of China, the Regulations for the Supervision and Administration of Medical Devices, the Provisions for Mandatory National Standards and the Provisions for Medical Device Standards, on July 7, 2020, NMPA issued the notice on matters related to further strengthening management for mandatory industry standards of medical devices, requiring drug regulatory authorities at all levels to effectively maintain the legal status of mandatory industry standards, further improve the mandatory industry standard system, promote the drafting and implementation of mandatory industry standards, reinforce the publicity, implementation and training, standardize the implementation of mandatory industry standards, and reinforce the evaluation on implementation of mandatory industry standards.