Services
Trialog’s experienced Import & Export department can handle all import regulatory requirements and customs release services.
According to the Israeli MoH regulations, all Investigational Medicinal Products for clinical trials must be released by a local QP.
Trialog’s xGXP compliant facility designed to maintain the integrity of all clinical trial materials is essential for the success of the clinical trial.
Trialog distributes clinical trial materials (CTM) to all hospitals and clinics in Israel.
Trialog has a dedicated GMP department for primary and secondary relabeling and repackaging.
Trialog offers its clients cost-effective local sourcing services for drugs, ancillary and equipment.
Trialog maintains a separate Quarantine/Destruction area for clinical trial materials returned for further storage, destruction or export according to client instructions.
