Clinical research is the bridge between the laboratory and the patient - the work of clinical researchers guarantees that new knowledge is quickly applied to benefit the patients, and that knowledge from the health care sector is applied in further research.

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

We can assist with our expertise throughout your project's entire life cycle - from study design to study report - in many types of clinical studies:

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

UCR offers a complete service covering initiation, planning, implementation, and reporting of local investigator-initiated studies as well as major international multi-centre trials. UCR is happy to assume responsibility for smaller and larger assignments in collaboration with academic institutions and individual researchers, as well as with pharmaceutical, diagnostic, and medical device companies of any size.

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