Medical Equipment
Agent Import of Class I and Class II Medical Devices
Agent Import of Class I and Class II Medical Devices
Detailed explanation of the regulatory requirements for exporting medical products to Spain, including customs clearance documents, special permits, CE certification, and AEMPS registration, as well as practical suggestions and risk control strategies.
为药品出口提供详尽的日本市场进入指南,包括基本流程、必要资质、认证过程,以及厚生劳动省的监管要求。
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