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Chinese Journal of Medical Instrumentation ; (6): 62-63, 2018.
Article in Chinese | WPRIM | ID: wpr-775553

ABSTRACT

According to the information of the supervision and inspection of in vitro diagnostic reagents for clinical use, this article analyzed the compliance issues and discussed the methods to solve the problems, to urge medical institutions to reduce the regulatory risk of in vitro diagnostic reagents in use.


Subject(s)
Government Regulation , Indicators and Reagents , Risk
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