“CD Log Management ensures that quality objectives significant to the requirements of customers and compliant with GSDP and GCP guidelines are identified and established at relevant levels within the organization.”
CD Log has an advanced Quality Management System that ensures storage, handling and distribution of investigational drugs in compliance with the international standards and guidelines for Good Storage and Distribution Practices.
Classified as a mid-sized drug depot in Lebanon by the Health Authorities, CD Log facility of 400 sqm for the warehouse and offices, is located in Beirut central district.
The warehouse is controlled by a Premises Control and Management System that ensures continuous monitoring and recording of temperature and humidity data, to guarantee optimal conditions for the storage of investigational drugs.
CD Log storage capabilities include:
- Controlled Room-Temperature: 15 to 25oC
- Regrigerated: 2 to 8oC
- Frozen: -25 to -15oC
CD Log uses its own fleet of vehicles for shipments and collections to and from sites. All vehicles are meticulously validated and equipped with GPS-technology, enabling real-time temperature and location monitoring.
A smooth and rapid distribution of clinical trial supplies to all areas within Lebanon is feasible within 2 working days.
All team attended the Essentials of Clinical Trials session at the American University of Beirut- Lebanon
Quality team certified as qualified internal auditors of QMS by APAVE- Lebanon
GCP certification of CD Log operations and quality teams
Executive team completed the Risk Management Certification.
Quality team certified as Internationally Qualified Clinical Research Auditor by IAOCR.
Acquisition of the Pharmacovigilance Certification.
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