We are aware of how important for our partners a swift Start-Up of a clinical trial is. We support our clients in organizing the preparatory phase of a clinical trial in a given country, aiming to achieve high efficiency in reducing the time window of protocol approval and the first visit of the first patient in the study. We check thoroughly the feasibility of a clinical trial in a country or region of Europe.

Our experience and a significant network of contacts of potential investigators help us assess the real possibility of study sites to recruit patients and optimize the process of choice, bearing in mind how important it is to obtain complete, accurate and reliable data from the study. We support our partners in the process of contracting sites as well as local vendors, and we are responsible for the research teams training process, preparing staff to conduct research in compliance with the protocol, ICH-GCP regulations, sponsor SOPs and local law regulations.