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。
The Quality System regulation outlines the minimum elements of a system for designing and producing a medical device.
质量体系法规描述设计和生产医疗器械最少体系要素。
It is not practical for a regulation to specify details of quality system elements for such a wide range of products.
对于如此宽泛的产品范围来说，一个法规规定具体的质量体系要素是不实际的。
It possess both the precise character of PID controller and the flexible advantage of fuzzy controller, and can guarantee the regulation system has good dynamic and static quality.
既具有PID控制器高精度的优点，又具有模糊控制器快速、适应性强的特点，保证了调节系统具有良好的动、稳态特性。
It possesses both the precise character of PID controller and the flexible advantage of fuzzy controller, and can guarantee that the regulation system has good dynamic and static quality.
既具有PID控制器高精度的优点，又具有模糊控制器快速、适应性强的特点，保证了调节系统具有良好的动、稳态特性。
The system of teaching management contains its group system, aim system of teaching management, its regulation system, and supervision and guarantee system in teaching quality.
教学管理体系包括教学管理组织体系、教学管理目标体系、教学管理制度体系、教学质量监控与保障体系。
Because the QS regulation covers a broad spectrum of devices and production processes, it allows some leeway in the details of quality system elements.
因为QS法规涵盖了宽泛品类的产品及生产流程，在具体的质量体系要素中允许某些偏差。
This manual will assist you in developing a quality system that meets the intent of the FDA Quality System regulation.
本手册会帮助你建立满足FDA质量体系法规意图的质量系统。
Abide by the regulation of ISO14001 and TS16949 and take the responsibility in security , environment and quality written in company system documents.
执行ISO14001、TS16949的相关条款，承担公司体系文件规定的相关（安全、环境和质量）责任。
The regulation process of a control system is one of the most important properties in appraising the quality of regulation.
自动调节系统的过渡历程是评价调节品质的一个重要特性。
The current Good Manufacturing Practices (GMP) requirements set forth in the Quality System (QS) regulation are promulgated under section 520 of the Food, Drug and Cosmetic (FD&C) Act.
质量体系法规所阐明的现行的GMP要求是在食品药品及化妆品法案第520节下所发布的。
The current Good Manufacturing Practices (GMP) requirements set forth in the Quality System (QS) regulation are promulgated under section 520 of the Food, Drug and Cosmetic (FD&C) Act.
质量体系法规所阐明的现行的GMP要求是在食品药品及化妆品法案第520节下所发布的。
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