负责医疗器械及药品包装材料的检验样品管理和检验标准、补充检验方法、技术服务等综合管理及相关统计工作。承担业务承接、分包、结果送达等工作。组织开展业务收费标准制定和日常业务收费核准。承担与相关技术单位的业务联系协调工作及客户服务工作。组织贯彻实施创新政策和产业政策。

　　组织开展医疗器械标准项目管理，实施标准宣贯、培训。负责医疗器械科研项目和成果管理，承担医疗器械重点实验室等科研创新载体的运行管理。组织实施技术能力建设等相关技术研究工作。

　　负责实习生及实习基地管理工作。既是中心与本院其它职能部门对接纽带，也是中心对外服务和联络的窗口。

　　Be responsible for the comprehensive management and related statistical work of medical devices and pharmaceutical packaging materials, including sample management and test standards, supplementary test methods, and technical services; undertake and subcontract business, and deliver results; organize the development of service charging standards, and approve routine service charges; be responsible for business contact and coordination with related technical units and customer service; organize and implement innovation policies and industrial policies.

　　Organize and carry out standard project management of medical devices, disseminate, implement and provide training on relevant standards; manage the research projects and achievements of medical devices, and undertake the operation and management of research innovation carriers of medical devices such as the key laboratory; organize and implement technical capacity building efforts and related technical research work.

　　Manage interns and practice bases. The Medical Devices General Business Department acts as a link between the Center and other functional departments of the Institute, and a window for the Center to serve and communicate with the outside world.

　　部门座右铭        行成于思，毁于随。