GMP Labeling & Manufacturing Activities
Trialog has a dedicated GMP department for primary and secondary relabeling and repackaging. In addition to helping our clients meet a variety of needs, we have recently added a range of manufacturing activities including over encapsulation, manufacturing of placebo capsules and Blinding/Randomization of kits. The department is managed by a Trialog pharmacist. It is inspected and approved by the Israeli MoH as GMP certified. Trialog’s expertise in performing a variety of relabeling operations means the lead time for delivery of clinical trial materials to sites can be kept to a minimum. We can also offer our clients label review services to make sure labels meet Israeli MOH requirements.