For Investigators

We can provide support in the conduct of ICH GCP compliant clinical trials to a large number of the sites in Ukraine working in different therapeutic areas. We train the site staff in ICH GCP to ensure Regulatory compliant study conduct at the site. We also provide training for Site Coordinators and prepare and integrate them into our global site management structure. We help sites to develop the recruitment strategy for each particular indication as well as mechanisms for their prompt implementation after site selection and initiation. After all necessary staff training and site preparation we can integrate you into our Site Management Organization and bring studies to your sites in addition to trials you receive from other CROs and Sponsors.

If you are not part of our Site Management Organization yet and would like to join us, please contact us for any further details.