CCBR recognises sponsor’s requirements to expedite clinical studies, to save costs and to drive efficiencies wherever possible into clinical studies. Below are two examples of where CCBR worked to reduce the number of screen fail rates compared to our competitors and non CCBR investigator sites.
Through using sound feasibility information, patient outreach and the CCBR Booking system, CCBR detailed significantly fewer screen failures across two large scale studies.
Working with CCBR speeds up and drives efficiencies in clinical trials by offering greater numbers of patients across fewer sites
A Global Footprint covering 16 dedicated Clinical Research Centers in high density population areas
Uniform SOPs enable the tightest possible adherence to study protocols and consistency across all CCBR sites
Real-Time tacking of subject enrolment and trial progress ensures sponsors have the most up to date information, all of the time
Centralised, standardised billing affords better visibility into trial costs for sponsors
