Being a part of Novolog Healthcare Group enables us to extend our offering to address more niches of the Clinical Trials ecosystem under the same roof.
Import (IoR) & Export

Trialog’s experienced Import & Export department can handle all import regulatory requirements and customs release services.

QP 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.

GMP Labeling & Manufacturing Activities

Trialog has a dedicated GMP department for primary and secondary relabeling and repackaging.

Local Sourcing

Trialog offers its clients cost-effective local sourcing services for drugs, ancillary and equipment.

Returns & Destructions

Trialog maintains a separate Quarantine/Destruction area for clinical trial materials returned for further storage, destruction or export according to client instructions.

More Services

Translation Services
Clinical trials are subject to stringent regulations and various approvals, which depend, to a large extent, on the quality of the translation that is submitted to the approving authority.
Decentralized trials services DTP/STP
Decentralized trials (DCT) becoming more dominant in clinical research during the last 2 years. One of the must attributes of DCT are home trials.