Clinical research is the bridge between the laboratory and the patient - the work of the clinical researchers is the guarantee that new knowledge is quickly applied to benefit the care sector, and that knowledge from the outside world is applied in research.

Robust clinical research is an essential prerequisite for medical advances that benefit patients and society as well as generating health-economic savings in the long-term.

We can assist with our expertise throughout the project's life-cycle - from the study design to the end of study reports - for the many different types of clinical studies.

  • clinical trials phases I-IV in accordance with ICH-GCP (International Conference of Harmonization - Good Clinical Practice)
  • observation studies
  • registry-based studies
  • medical device studies

UCR offers a complete service covering initiating, planning, implementing and reporting for local investigator initiated studies as well as major international multi-center trials. UCR is happy to assume responsibility for smaller and larger assignments in collaboration with academic institutes and individual researchers, as well as major and minor pharmaceutical, diagnostic and medical device companies.

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