Facilities
Trialog’s facilities are MoH-approved and GDP-certified for storage and distribution of drugs at all temperature categories.
Trialog's operates GMP-certified labeling rooms.
Trialog's operates GMP-certified labeling rooms.
Trialog’s main facility currently provides storage in the following categories:
Ambient
(15 -25°C)
Refrigerated
(2-8°C)
Frozen
(-20°C)
Deep Frozen
(-80°C)
Controlled Drugs
Cryogenic
Trialog’s secondary BCP back-up facility provides storage in the following categories:
Ambient
(15 -25°C)
Refrigerated
(2-8°C)
Frozen
(-20°C)
Deep Frozen
(-80°C)
Safety & Security
Efficiency and product security
To maximize efficiency and product security, Trialog uses it’s Novolog group fleet of validated vehicles for site deliveries, all equipped with sophisticated temperature monitoring systems.
BMS
A validated Building Monitoring System (BMS) is used with multiple sensors throughout the warehouse located according to a mapping program to monitor temperature and humidity. On line data measurements are recorded every minute. The BMS live system issues alerts for any discrepancy observed allowing shortest possible reaction time in case of need.
Backup systems
Understanding the sensitivity of clinical trial material storage needs, Trialog has in place the necessary backup systems for risk management control.
Drug Accountability
Trialog can track the supply chain of the product down to the kit level from the moment the medication arrives at Trialog till it is delivered to site and returned to Trialog as required.
