Fact sheet

  • Clinical Trials Management and Logistics Department was established in 2004.

  • GMP, GCP, GDP, local regulatory standards and Interfarmax internal SOPs compliance
  • ISO 9001 standardization of service
  • Pharmaceutical license, Pharmaceutical license for controlled drugs
 
  • 130 studies has been carried out
  • 39 active studies
  • 29 foreign CRO/ Sponsors
  • 100 shipments to sites on average per month

 

  • More than 50 sponsor audits successfully passed
  • 5MoH Inspections passed,  no gross violations and critical findings,
  • 3 ISO 9001 accreditations by Bureau Veritas successfully passed, Bureau Veritas annual inspections for ISO requirements compliance

  • Client-oriented project management team meeting each exceptional requirements
  • Trained and experienced staff

  • Constant 24/7 temperature and humidity online monitoring (ambient, cold, frozen)
  • Automated alarm notifications of any temperature deviations
  • Separate incoming and outgoing routes
  • Controlled access, 24/7 secure and safe storage