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.