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. We also offer publication management and Clinical Event Adjudication (CEA). 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) 

For more information please contact 
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Director Clinical Research 

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