CCBR uses proven recruitment strategies to quickly fulfill subject population targets across fewer sites for more efficient subject enrollment. Our database of over 200,000 potential subjects, each with a detailed clinical history, greatly enhances the speed and accuracy of subject selection. In addition, our clinic managers have an expert understanding of the communities from which to recruit subjects, and routinely exceed enrollment and retention targets.
All CCBR trials are performed at sites either fully owned by CCBR or run by CCBR partners. Our strategic network of 10 clinics can reduce the cost of drug development and accelerate product time to market by providing dedicated clinical-trial services and a database of qualified participants.
CCBR provides a single point of contact for overall study management and administration for all trial locations. We coordinate clinical-site initiation efforts, conduct prestudy activities, track performance against enrollment targets and overall site performance, and ensure that all sites are qualified, staffed, and equipped to manage all study activities. Because all aspects of a study are handled uniformly across all clinics, CCBR makes it easier to manage your clinical trials.
CCBR provide clinical and technical oversight of all study-related activities, develop in-depth reporting to extract the most scientific value, facilitate submission of trial data to regulatory agencies, and assist in identifying potential publication or collaboration opportunities.
Since 1992, CCBR has provided direct, hands-on management of clinical trials. Our services include all aspects of a clinical-study program, from site prequalification, site initiation, subject screening, randomization, ongoing data collection, and reporting to final data submission. Our program-tailored management services ensure that your clinical trial adheres to study protocols and that all compliance matters are in order.
CCBR collects, tracks, analyzes, and reports on all study-related activities. Our staff works collaboratively to ensure study requirements are documented, and that all system deployment efforts are completed accurately and validated on time. In addition, our technical staff safeguards and preserves data security and confidentiality across sites and throughout data collection, analysis, and reporting. Committed to absolute compliance Every year, our sites undergo 10 to 15 inspections from the FDA, EMEA, local authorities, sponsors, and CROs.
At CCBR, we work collaboratively and seamlessly with our clients to assist in quickly developing new and effective therapies that respond to the ever-changing medical needs of a growing world population. Over the years, we have partnered with industry leaders to bring numerous leading compounds to market across a broad spectrum of therapeutic areas. Working with us means collaborating with an experienced partner equipped to perform whatever role is needed in your clinical-trial program.
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
