training surveys meaning in Chinese
培训调查
Examples
- Results : training survey of adverse effects of medical devices was the base to development survey . training work should accord as requirements of training
结果作为医疗器械产品上市后监管的主要手段,医疗器械不良事件监测在全世界开展的时间不长,是一个新的领域。 - Factors improving the occurring of the requirements for training survey of adverse effects of medical devices in our country included following : the characters of adverse effects of medical devices and training itself , the current conditions of survey of adverse effects of medical devices and the corresponding training , the successful experiences of development survey of adverse effects of medical devices in developed countries and the practical requirements by employees involved in medical devices
我国的医疗器械不良事件监测刚刚起步,借鉴了发达国家的经验,但国内外对医疗器械不良事件监测培训的研究进行得较少,尤其是培训需求研究更少,迫切需要开展培训需求研究作为培训工作的依据。医疗器械不良事件和培训本身的特点、有关从业人员的现实需求、我国医疗器械不良事件监测及其培训的现状以及发达国家开展医疗器械不良事件监测的成功经验促成了我国医疗器械不良事件监测培训需求的产生。 - Purpose : to study the requirements for training survey of adverse effects of medical devices , detect the weak points in current work about training survey of adverse effects of medical devices , discuss the more efficient training fashions and methods , and provide references and suggestions for establishment more rational training project
目的对医疗器械不良事件监测培训需求进行研究,分析目前医疗器械不良事件监测培训工作的薄弱环节,探讨更加高效的培训方式与方法,为制定更加合理的培训方案提供参考和建议。 - Methods : to study the current condition requirements for training survey of adverse effects of medical devices , development the investigation and study the current condition of enterprises manufacturing / managing medical devices , supervise department and personnel involved in medical organizations , statistic analysis were used also . synthetical analysis the results of theoretical studies and current investigation were taken
方法对医疗器械不良事件监测和培训的现状进行研究;开展对医疗器械生产经营企业、监管部门以及医疗机构有关人员的现状调查,并进行统计学分析;结合相关理论综合分析讨论了现状调查的结果。 - The major subjects of training survey of adverse effects of medical devices were enterprises manufacturing / managing medical devices , medical organizations and staff in supervise department . , the requirements for training survey of adverse effects of medical devices to whom were same or specific in the content , temporal limits , modes or methods and so on
医疗器械生产经营企业、医疗机构和监管部门的有关人员是医疗器械不良事件监测培训的主要对象,对于医疗器械不良事件监测培训的内容、时间时限、方式方法等有关事项有着相同或不同的需求。