We conduct design and management of clinical trials of phases I-IV of commercial / non-commercial, non-interventional studies and research projects.

We take over complete preparation and submission to higher federal authorities and ethic committees as well as submission to local authorities.

With our team of long-term experienced trial coordinators we maintain all ongoing processes during a clinical trial.

With our team of long-term experienced clinical monitors we cover all parts of monitoring nationwide.

With our team of experienced scientists we create texts in an accurate and competent manner and conduct literature researches.