UCR´s competent and skilled Clinical Operations team offers support and services throughout the full
life cycle of your clinical study or trial - from initial study design and protocol development to clinical study reporting
Our experienced team are knowledgeable in conducting both observational studies, in collaboration with regional, academic, or independent researchers, as well as large, global, complex, randomized clinical trials together with global medical corporations, in pharmaceuticals and medical devices. (e.g., RCT, R-RCT studies)
Read our brand-new consolidated knowledge document describing Decentralized Processes in Clinical Trials (DCT). It has been developed by a working group consisting of representatives from Uppsala Clinical Research Center, Region Stockholm, and Lif – the research-based pharmaceutical industry.
Decentralised Processes in Clinical Trials (DCT)
For more information please contact
Director Clinical Research