Medical device-Quality的意思|示意
医疗器件质量
Medical device-Quality的网络常见释义
医疗器械质量办理体系用于法规的请求 ... SO13485：2003规范的全称是《医疗器械质量办理体系用于法规的请求》（Medical device-Quality management system-requirements for regulatory）。
Medical device-Quality相关短语
1、 Medical device-Quality management system-requi 医疗器械
2、 Medical device-Quality m 医疗器械
3、 Medical Device Quality Syst 医疗器械质量体系手册来源
Medical device-Quality相关例句
Its very important on the quality assurance in feasibility demonstration of medical device, this paper study quality control of the medical device in feasibility demonstration from all its aspects.
医疗设备的可行性论证对其质量保证是非常重要的，现从多个方面探讨了医疗设备可行性论证质量控制。
These requirements include establishment registration, medical device listing, quality system, medical device reporting, premarket approval or clearance, labeling and U. s. agent requirements.
这些规定包括工厂的注册，医疗设备清单，质量系统，医疗设备报告，售前批准或者认可，商标及美国代理的要求。
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。
Conclusion The QC program of PACS image display device is an essential to ensure high-quality in digital medical environment.
结论PACS图像显示器的质量控制是确保数字化医疗环境优质性的重要措施。
Each manufacturer shall establish and maintain a quality system that is appropriate for the specific medical device (s) designed or manufactured, and that meets the requirements of this part.
每个工厂应建立并保持一个质量体系是适宜的特定医疗器械的设计或制造的，并且符合要求的这一部分。
Meeting US and European Supplier Control Requirements. Medical device manufacturers operating under European quality...
医疗器材厂商该如何符合美国与欧洲对承包商管制的要求。