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With regard to the issuance of Medical Device Adverse Event Monitoring and re-evaluation of management practices (for trial implementation) notice 2009-08-12
On the reagent system of assessment criteria 2009-08-12
Clinical study in vitro diagnostic reagents technical guidelines 2009-08-12
The production of in vitro diagnostic reagents Rules 2009-08-12
In vitro diagnostic reagents prepared statement guiding principles 2009-08-10
Registration of Medical Device Regulations 2009-08-19
Medical equipment manuals, labeling and packaging identification regulations 2009-08-19
Medical Device Good Manufacturing Practice (Trial) 2009-08-19
Supervision and Administration of Medical Device Manufacturing 2009-08-19
Medical Device Enterprises license management approach "(Board Order No. 15) 2009-08-19
Supervision and Regulation of Medical Devices 2009-08-19
Standard management practices for medical devices 2009-08-19
In vitro diagnostic reagent system for assessing the implementation of the provisions of 2009-08-19
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