Knowledge Base
Expert guides, regulatory references, procurement best practices, and technical documentation for medical product trade between China and international markets.
CE Marking for Chinese Medical Devices: What Importers Need to Know
A complete guide to CE marking requirements for medical devices manufactured in China. Covers EU MDR compliance, notified body selection, technical documentation, and common pitfalls.
CT Scanner Buyer's Guide: Slices, Brands, and Pricing for 2026
Everything you need to know before purchasing a CT scanner — slice count selection, brand comparison (Chinese vs global), AI integration options, installation requirements, and total cost of ownership.
Understanding Incoterms 2020 for Medical Device Trade
FOB, CIF, DDP, and more — learn which Incoterm protects you best when importing medical devices from China. Includes practical examples and cost comparison.
ISO 13485 Quality Management for Medical Device Manufacturers
A technical overview of ISO 13485 requirements for medical device manufacturers. Covers documentation, process control, risk management, and audit preparation.
Medical Device Import Regulations by Country: Southeast Asia 2026 Guide
Country-by-country guide to medical device import regulations in Southeast Asia — covering Indonesia, Vietnam, Thailand, Philippines, and Malaysia.