The completion timeframe of a clinical trial is always a determining factor for its success. The awareness of that helped us focus on what we believe mainly defines the study timelines:
Site Feasibility & Selection
Our wide Investigator database along with our knowledge and experience give us the strategic advantage of being able to select the right investigational sites which will allow us to ensure an on-time site initiation and study completion. The proper site identification and selection is crucial for us as it has a critical impact on both recruitment rate and generation of quality data. Over a lengthy list of experienced investigational sites we select those that will be able to respond adequately to your study's requirements.
Start Up & Site Activation
As the regulatory environment is driven to change, the challenges the clinical trial industry is experiencing during the initiation of a study are continuously increasing. Our Study Start Up specialists are always up to date with the national and international legislation developments so as to ensure quality compliance in all local regulatory activities. What makes us so competitive, however, is the ability to reduce the time from cost proposal acceptance to study activation and enrolment start.