Eurotrials has Phase I-IV experience across various therapeutic areas.
With more than 20 years’ experience in the industry, we achieve the best results for your project by providing you the integrated support of a full-service CRO. Our multidisciplinary team includes Project Managers, Clinical Research Associates, Study Start-Up and Regulatory Specialists, Data Managers, Statisticians and Medical Writers, all of whom are focused on building solid relationships with experienced research centers in various therapeutic areas and countries, which is a key factor in successful patient recruitment.
In some specific complex therapeutic areas, such as Oncology, operational and regulatory expertise coupled with experienced research centers are crucial factors to the project’s success. Our operational experience (from the CRA to the Medical Writer), together with our specialized Start-up Team fully dedicated to regulatory submissions, facilitates the study implementation phase.