CEBIS’s established Canadian presence can support clinical research programs requiring coordination across clinical operations, study logistics and the organization’s broader international delivery network.
2201 Drew Road
Mississauga, ON L5S 1E5
Canada
CEBIS can coordinate Canadian clinical research activity with relevant functions across the study lifecycle.
CEBIS supports sponsors conducting clinical trials in Canada through access to a Canadian site network and clinical operations support. We help assess site feasibility, plan recruitment, coordinate study start-up and oversee trial conduct according to each protocol.
CEBIS offers clinical trial logistics as a separate service delivery. Depending on the study, support may include clinical supply planning and management, trial material labelling and packaging, international shipping and site deliveries, shipment tracking, consumables resupply, and temperature-controlled packaging, storage and transport. The applicable services, responsible entity and delivery arrangements are agreed for each project.
For programs involving both Canada and the United States, study activities can be coordinated around common project leadership while respecting the requirements of each participating market.
Canada Sites
→ U.S. Operations
→ Regulatory Coordination
→ Clinical Supply
→ Data & Safety
→ Sponsor Oversight
Tell us about your study, products, countries, participating sites, packaging requirements, temperature needs and timeline. A member of the CEBIS team can discuss the appropriate supply and logistics approach.