1984年FDA被授权建立一个医疗器械强制报告系统（MDR System），这个系统要求医疗器械制造商和进口商向FDA报告导致死亡的、严重伤害以及器械故障引起的不良事件。
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mdr medical device reporting system 医疗器械报告系统
The global threat of MDR-TB and XDR-TB (M/XDR-TB) can be halted if TB control measures are urgently put in place across the whole health system as recommended under the Stop TB Strategy.
如果按照控制结核战略的建议在整个卫生系统中紧急采取结核病控制措施，就可制止耐多药结核病和广泛耐药结核病的全球威胁。
If a manufacturer has a quality system as required by the QS regulation, the frequency of MDR reporting should be minimized.
如果制造商有符合QS法规的质量体系，MDR报告的频率会是最少的。
Drug delivery system (DDS) is a novel approach to overcome multidrug resistance (MDR) in tumors nowadays.
药物递送系统是克服肿瘤多药耐药性(MDR)的一种新策略。
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