ABSTRACT
Through the analysis of the current status and problems of innovative medical devices evaluation, tnis paper discussed the strategies of evaluation, and ultimately raises the frame of evaluation, so as to provide reference for scientific evaluation of medical devices in China.
Subject(s)
China , Equipment and Supplies , Reference Standards , Evaluation Studies as TopicABSTRACT
Medical tourism has grown into a booming market worldwide,which however remains at a startup stage in China given its fast development in recent years.This paper probed into the present status of medical tourism at home and abroad,discussed key roadblocks to tackle for medical tourism,including government regulations,medical resources,international certification,promotions and marketing,language barriers,and visa.On such basis,the authors come up with the following recommendations:enhance policy support and complete the governance of medical tourism; tap resources of public hospitals and encourage private involvement; encourage international certification of medical institutions to explore overseas medical tourism; encourage tourist firms to develop medical tourim products and promoting medical tourism; build brands and complete product lines.
ABSTRACT
Medical device software is a special kind of medical device, which is different from hardware and may introduce more risk. How to reduce the risk of software efficiently is the important thing for medical device regulation system. This article analyzes medical device software's properties, introduces the status of foreign supervision, and finally gives some advises to the related parties.
Subject(s)
Equipment and Supplies , Reference Standards , Organization and Administration , SoftwareABSTRACT
The invention and use of science and technology have always been a double-edged sword. The paper analysed the function and influence of medical hi-tech on medical and health undertakings development in China, and gives opinions on how to treat medical hi-tech correctly, so as to provide reference for the use and supervision of medical hi-tech.