The completion timeframe of a clinical trial is always a determining factor for its success. The awareness of that helped us invest on what we believe mainly defines the study timelines:

Investigational Site Feasibility & Selection

Our wide Investigator database along with our in-depth knowledge and experience give us the strategic advantage of being able to select the right investigational sites for each clinical study, 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 patient 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, making sure that clinical trial's recruitment milestones will be timely achieved.

Study Start Up & Site Activation

As the regulatory environment is constantly evolving, the challenges the clinical trial industry is experiencing during clinical study initiation are continuously increasing.

Our Study Start Up specialists are always up to date with the national and international legislation developments 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.