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
  • GDP standardization of service
  • Pharmaceutical license, Pharmaceutical license for controlled drugs

 

  • 140 studies has been carried out
  • 40 active studies
  • 30 foreign CRO/ Sponsors
  • 120 shipments to sites on average per month

 

  • More than 50 sponsor audits successfully passed
  • 7 MoH Inspections passed,  no gross violations and critical findings,
  • GDP and ISO 9001 accreditations and annual inspections by Bureau Veritas since 2012 successfully passed

 

  • 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