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

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

Cost

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

Recall

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

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

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)

 

Sourcing

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)

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

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