Eurotrials has Phase I-IV experience across various therapeutic areas, as depicted below. With more than 20 years in the industry, we successfully achieve the best results for your project, through integrated project team capabilities and resources. Our multidisciplinary project teams include Project Managers, Clinical Research Associates, Study Start-Up and Regulatory Specialists, Data Managers, Statisticians and Medical Writers that provide the integrated support of a full-service CRO.
In some specific complex therapeutic areas, operational and regulatory expertise coupled with experienced investigational sites are crucial factors to the project’s success. Our operational experience (from the CRA to the Medical Writer) together with a specialized Start-up Team fully dedicated to regulatory submissions, aims at facilitating the study implementation phase. Also, our project teams are focused on continuously building solid relationships with experienced investigational sites across several therapeutic areas and countries which is a key factor patient recruitment success.