Processes

  • Operate under proven SOP’s which have undergone multiple customer audits and an FDA inspection.
  • Developed systems of high level accountability and traceability within our kit assembly.
  • Offer design and development assistance for customized specimen collection kits.
  • Offer guidance from trained staff in the area of DOT/IATA/ICAO dangerous goods regulations with regards to biological substance packaging.
  • Assembly of sterile and non-sterile specimen collection kits.
  • Warehousing and distribution.
  • Monitored climate controlled storage rooms for temperature sensitive components.
  • Emphasis on superior customer service.