Agent Import of Class I and Class II Medical Devices
Analyze the compliance requirements for the return and repair of imported medical devices, discuss the difficulties in customs clearance and the restrictions on bonded area repairs, and provide alternative solutions.
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.
Provides a comprehensive guide to entering the Japanese market for pharmaceutical exports, including basic procedures, necessary qualifications, certification processes, and regulatory requirements from the Ministry of Health, Labour and Welfare.
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PSB Record: Shanghai No.31011502009912
