欧盟医疗器械标准管理体系由指令、协调标准以及符合性评估程序组成。
Medical devices standards system in EU is composed of directive, harmonized standards and conformity assessment procedures.
组织应建立并维持文件化程序，以定期评估其与相关环境法令与规章之符合性。
The organization shall establish and maintain a documented procedure for periodically evaluating compliance with relevant environmental legislation and regulations.
组织应建立并维持文件化程序，以定期评估其与相关环境法令与规章之符合性。
The organization shall establish and maintain a documented procedure for periodically evaluating compliance with relevant environmental legislation and regulations.
应用推荐