Streamlining Cargo Reallocation Cuts Demurrage Boosts Efficiency

Streamlining Cargo Reallocation Cuts Demurrage Boosts Efficiency

The cargo re-allocation process after inspection involves obtaining a Non-Shipment Certificate, submitting a re-allocation application, and canceling/re-declaring customs. This article details the key operational points of each step, providing strategies for cost control and handling special circumstances. It aims to help freight forwarding companies efficiently complete re-allocation, reducing the risk of port detention. The process includes understanding the necessary documentation and procedures for successful cargo re-allocation.

Guide to Releasing Detained EMS Shipments at Customs

Guide to Releasing Detained EMS Shipments at Customs

Don't panic if your EMS package is detained! This article delves into the common reasons for EMS package detention, such as prohibited items and inaccurate declarations. It provides three major strategies: personal declaration and tax payment, commercial customs declaration, and application for return. It also emphasizes the importance of real-time tracking of processing progress and utilizing rights protection channels to safeguard your interests. This helps you quickly resolve the issue and successfully clear customs.

Importers Face Rising Demurrage Costs Seek Solutions

Importers Face Rising Demurrage Costs Seek Solutions

This article delves into the common issue of demurrage in international trade, distinguishing it from detention fees. It details the calculation methods for demurrage and provides three effective strategies to avoid it. Furthermore, it clarifies the difference between port storage charges and demurrage, explaining the operational principles of the demurrage mechanism. The aim is to assist foreign trade enterprises in effectively controlling costs and improving profitability by understanding and managing these charges.

NMPA Issues Guide to Medical Device Registration in China

NMPA Issues Guide to Medical Device Registration in China

The People's Republic of China Medical Device Registration Certificate is a crucial market access permit for medical devices entering the Chinese market. This article interprets the importance of the registration certificate and emphasizes the role of compliance procedures, professional agencies, and customs clearance services in successfully obtaining the certificate, helping companies smoothly enter the Chinese market. It highlights the need for adherence to regulations and the benefits of utilizing expert assistance to navigate the registration process efficiently and effectively.