This article provides an in-depth analysis of the latest regulatory requirements for pharmaceutical equipment imports in 2025, revealing three major compliance risks in medical device classification, technical standard certification, and certificate of origin, while offering selection criteria for professional customs brokers and comprehensive operational guidelines.
This article reveals six common misjudgments companies make when selecting German equipment import agents, using customs data comparisons and practical cases to analyze key operational points including qualification verification, tax treatment, and technical barriers.