Owing to the years of cooperation with experienced investigators and leading experts, our CRAs select top clinical trial sites and assist the sites in securing the agreed number of subjects, with a high quality of data.
We have a long-standing cooperation with regulatory authorities, medical institutions and other key partners. We use our in-depth knowledge of professional standards and local particularities to provide services of regulatory submission, initiation and monitoring patient recruitment in clinical trials.
We are dedicated to:
Maintaining long term cooperation and support of investigational sites
Working in line with ICH-GCP standards and local regulation
Achieving business goals set by Sponsor
Providing continuous training for our personnel
Offices in Croatia: