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.
為藥品出口提供詳盡的日本市場進入指南,包括基本流程、必要資質(zhì)、認證過程,以及厚生勞動省的監(jiān)管要求。
? 2025. All Rights Reserved. 滬ICP備2023007705號-2 PSB Record: Shanghai No.31011502009912