WHO regards trial registration as the publication of an internationally-agreed set of information about the design, conduct and administration of clinical trials.
WHO将试验注册视为有关临床试验设计、过程和管理的国际公认信息设定的发布。
That person should be responsible for the trial registration data set and for making sure that the same data is provided to each registry.
联系人应负责试验注册数据集,并保证向每个注册中心提供该数据。
Event scheduling, user registration and initial avatar set-up must be automated. Much of this has been implemented.
活动安排、用户登记和初始角色设置必须被自动化,其中大部分目标已经实现了。
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