CD Log maintains Investigational Medicinal Products integrity through an adequate and efficient Quality Management System.

We rely on our attention to detail and on our understanding of the critical impact time has on the flow of goods to meet our customers' needs and to ensure product integrity.

What can CD Log add to handling your CT supplies?


Supply Chain Integrity

More than 2,900 shipments to sites with less than 0.5% temperature excursion


Annual validation of packaging material and vehicles


Coordination with clearing agents, all local freight forwarders, and couriers


Timely & Cost Effective Services

Less than 24-hour lead-time for shipments to sites covering the Lebanese territory


93% customer satisfaction rate as a key indicator of services’ cost-effectiveness


Site Logistics Workload Decrease

Coordination with pharmacies of more than 15 sites in order to adapt to their needs


Relief of sites from stock management burden: storage, stock counts, and reconciliation


Site logistics support


Logistics Services


Storage & Distribution

240 sqm monitored and controlled cold and ambient storage areas (Temperature & Humidity)


Frozen storage service available in 2021


Sourcing of calibrated single-use temperature monitoring devices upon request


Temperature-controlled shipments to sites


Return of IMP from sites, Stock reconciliation at depot and Preparation for IMP re-exportation (packing and labeling)




Stock Management

Automatic daily stock reporting with 100% stock accountability accuracy


Drug and Supplies receipt, distribution, return management, and final stock reconciliation


Handling of Interactive Response Systems (IRS)



Local sourcing of non-IMP

Purchase of non-IMP (Comparators, SOC, Ancillaries, and thermometers...) from Lebanese market, whenever available


Handling stock management and shipments to sites of all kind of ancillaries


Return of non-IMP from sites, Stock reconciliation at depot and Preparation for re-exportation (packing and labeling)


Over-Labeling Activity

CD Log is authorized by Law to over-label IMPs for a shelf-life extension at the depot


More than 15 over-labeling activities performed to date on 20,000 units at CDLog warehouse

Document Control & Archiving

Equipped area of 50 sqm for archiving of study documents


25-year retention period for study documents


Destruction of Clinical Trial Supplies

Destruction of IMP using an external provider in a European country and issuance of a destruction certificate


Local Destruction of unused ancillaries and issuance of a destruction certificate