At UCR we can contribute our expertise throughout the project, in many different types of clinical studies, from study design to final study report.

• phase I-IV clinical trials in accordance with the International Conference of Harmonization - Good Clinical Practice (ICH-GCP)
• observational studies
• register-based studies
• medical technology studies

We provide complete service to initiate, plan, implement and report both local research-initiated studies and major international multicenter trials. We take responsibility for both large and small assignments in collaboration with academic institutions and individual researchers such as pharmaceutical, diagnostics and medical technology companies.

We provide assistance with Suspected Unexpected Serious Adverse Reaction (SUSAR) reporting in projects run by us.

As a non-profit academic research organization, we offer access to UCR's skills at affordable prices for academic researchers. 

For more information please contact 
Katarina Durk Boustedt
Director Clinical Research 
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