Editorial Note: This article is written with editorial review and topic relevance in mind.
The nmpa requires clinical data for all class ii and class iii devices, unless the device appears in one of the regulator’s published clinical evaluation exemption lists. 中国国家薬品監督管理局＜national medical products administration (nmpa)> であり、中国で販売するすべての医療機器、医薬品、医薬品包材、化粧品、保健食品の審査認.
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