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BEIJING, April 9 (Xinhua) -- China's State Food and Drug Administration released a circular on Tuesday calling for strengthened supervision1 over the quality of medical equipment used in the diagnosis2 and treatment of H7N9.
The circular urged local health departments to monitor the production status and sales records of medical equipment production companies within their jurisdictions3, especially in regards to protective apparel, respirators, anesthesia machines and diagnostic reagents, among other equipment.
Health departments were also told to launch campaigns to check local medical equipment manufacturers for effective quality control systems, valid4 registration5 certificates for their products, adequate management of source materials and officially-approved labels and manuals.
While vowing6 severe punishments for illegal production and sale activities, the administration urged local health departments to focus on the research and development of in vitro diagnostic reagents for the H7N9 virus and ensure that developers and manufacturers of such products apply for product registrations7 in accordance with laws and regulations.
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1 supervision | |
n.监督,管理 | |
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2 diagnosis | |
n.诊断,诊断结果,调查分析,判断 | |
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3 jurisdictions | |
司法权( jurisdiction的名词复数 ); 裁判权; 管辖区域; 管辖范围 | |
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4 valid | |
adj.有确实根据的;有效的;正当的,合法的 | |
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5 registration | |
n.登记,注册,挂号 | |
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6 vowing | |
起誓,发誓(vow的现在分词形式) | |
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7 registrations | |
n.登记( registration的名词复数 );登记项目;登记(或注册、挂号)人数;(管风琴)音栓配合(法) | |
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