We organize a distribution of the investigational medicinal products (IMPs) for clinical studies, assuring that IMPs are delivered to clinical sites under appropriately controlled conditions. We verify if distribution of medicinal products to individual sites is executed in line with existing law and GMP/GDP recommendations. We keep an eye on the whole process of product distribution from manufacturing facility to the clinical research centre by control of shipping companies, transport conditions or the policy of goods identification.

We also offer investigational medicinal products for clinical studies re-packaging coordination in compliance with GMP.

We deal with sourcing of reference medicinal products for R&D studies and for clinical trials – both from EU and from third countries. Health-Med assures that all the activities connected with reference product sourcing, together with transport organization under controlled conditions are appropriately handled.