Reach your recruitment and study goals in an expedited timeframe

For larger trials or subject populations that are difficult to recruit from one location, reach your recruitment goals and accelerate trial timelines with multi-centre trials.

Capabilities include:

• Identifying the need for a multicenter clinical trial and determine the number of centres to complete the trial
• Designing of multi-centre studies
• Identifying the suitable clinical trial sites and investigators for conducting the multi-centre clinical trial
• Electronic data capture system for uniformity of data collection among the sites
• Coordinate the sites and manage the overall study to successfully complete the study in compliance with ICH-GCP and required regulatory guidelines