Based on its wealth of experience in the pharmaceutical sector, our team has quickly devised product management processes, which are approved for pharmaceutical purposes.

GDP regulations applied by Eurotranspharma Benelux include:

  • A quality manual, which is documented, updated and managed by the operators and management
  • Standardised and validated equipment: vehicles, cooling systems, telematics, depots
  • Redundant and centralised transport management system (PDA/TOKS)
  • Maintenance contracts for the entire infrastructure
  • Drivers trained in the relevant good practices for the sector, in full compliance with the European Guidelines for Good Distribution Practices of Medicinal Products for Human Use (2013/C 343/01)
  • Employees backgrounds checked
  • Employee driver ID
  • Strict and robust procedures executed by a flexible team
  • Traceability of vehicles, temperatures and keeping records over several years
  • Non-conformity management and CAPA plan
  • Audits conducted in house, by customers and the Federal Agency for Medicines and Health Products (FAMHP)

 

tpb temp tolerance