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About CMDRD
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2016
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Main Enabling Legislation
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Regulations
2015
Use
Administrative Measures for Quality Supervision on the Use of Medical Devices (CFDA Order No.18 2015)
2012
Use
Centralized procurement specification for A class large medical equipment(MOH notice No. 96 2012)
2012
Use
Centralized procurement specification for high-value medical consumables(MOH notice No. 86 2012)
2010
Use
The Safety Management Practices for Medical Device Clinical Use(MOH notice No. 4 2010)
2011
Use
Administrative Measures for Medical Equipment of Medical Organisation(MOH)
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