Working with CCBR speeds up and drives efficiencies in clinical trials. CCBR recruits significant numbers of patients through our network of dedicated Clinical Research Centres, in greater numbers than can be achieved through using ‘non CCBR investigator sites’, which in turn offers significant and recognisable cost & time savings across clinical studies and programs, as well as offering cost savings associated with sponsor’s internal costs for conducting trials.
A Global Footprint covering 16 dedicated Clinical Research Centers, spanning 10 countries including, Denmark, Poland, Czech Republic, Romania, Estonia, Lithuania, China, Hong Kong, Brazil, Argentina and Peru
Uniform SOPs enable the tightest possible adherence to study protocols
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
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
