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.
We offer a comprehensive portfolio of services which cover all administrative and regulatory aspects of clinical I-IV phase trials as well as non-interventional trials and research projects. In accordance with your individual requirements we manage all processes of a clinical trial from design, conduct and monitoring to analysis or take over only individual tasks within the context of clinical trials.
- Design / Project management
- Submission to regulatory authorities
- Trial coordination
- Medical writing
- Data management / Biometry
- Indication expertise / Experience
individual solutions, targeted to your projects
flexible management of a clinical study / support in the scientific area – full service or sections
personal obligation of our employees towards your project
highly-qualified, experienced personal
quick processing and adjustment to new conditions