Ensuring that all products entering a country meet local legal and documentation requirements, including customs declarations, permits, tariffs, and quality records, is essential to global clinical trial logistics.
This compliance enables investigational products to be imported, stored, and distributed smoothly, avoiding delays or the risk of seizure. Import and export controls apply at global gateways and regional depots whenever clinical or commercial products cross international borders for storage or distribution. This includes the initial import of investigational products or comparators into a study region, as well as exports to investigator sites, depots, or manufacturers for analysis or destruction. In countries where the sponsor has no local legal presence, We will be your Importer of Record to ensure compliant entry and customs clearance.