Drug import and export services
Today, with the increasing popularity of multi center clinical trials worldwide, the cross-border circulation of drugs faces strict regulatory requirements and complex operational processes.
We help our clients ensure the safe, compliant, and efficient entry of research drugs into the Chinese and other markets through our professional import management experience and comprehensive compliance system.
Import and export planning
Import strategy design: Develop the optimal import and export plan based on clinical trial protocol requirements, drug properties, and regulatory requirements.
Document preparation and filing evaluation support: Assist clients in preparing the necessary documents for import and export.
Customs clearance path and time assessment: Intervene in supply planning at the early stage of the project to help customers evaluate customs clearance paths, cycles, and potential risks, and optimize timelines.
Import execution and regulatory coordination
Drug Import&Export clearance service: Acting as an agent to complete customs declaration, drug regulatory filing, and port inspection Regulatory requirements for handling special categories of drugs (cold chain, biological products, etc.) Provide support for comparing Chinese and English materials, label review, and filing
Communicating and coordinating with regulatory agencies: representing clients to communicate with drug regulatory departments, customs, and inspection and quarantine agencies to ensure material compliance and smooth processes Provide localized policy interpretation and operational execution for international pharmaceutical companies.
Temporary import and export management: Establish a traceable import batch and quantity management system for multiple batches and multi center clinical trials.