CCBR is a specialist organization involved in clinical research and clinical studies. CCBR accesses and recruits patients for clinical trials and conducts studies at dedicated Clinical Research Centres located in strategic locations around the world where there is great potential to recruit large patient numbers across many different therapeutic areas.
Significant and recognizable time and cost savings across clinical studies and programs, through CCBR recruiting patients more quickly and in greater numbers at each research centre, when compared to single investigator sites.
CCBR is based in Copenhagen, Denmark and operates 16 Clinical Research Centres in Denmark, China, Hong Kong, Brazil, Peru, Argentina, Poland, Czech Republic, Estonia, Lithuania and Romania.
Each Clinical Research Centre offers highly trained and experienced staff, with each staff member knowledgeable in aspects of what is required to conduct a successful clinical trial and also experienced and well trained in ICH GCP and CCBR’s Global SOPs. In-house experts have working knowledge of current, country & region specific regulatory guidelines and expectations regarding protocol development and execution.
Rapid, localized subject recruitment CCBR uses proven recruitment strategies to quickly fulfil subject population targets across fewer sites for more efficient subject enrolment. CCBR’s database contains information for over 300,000 potential subjects, offering information covering detailed clinical histories. This ‘in-house’ information greatly enhances the speed and accuracy of subject selection. In addition, CCBR clinic managers have an expert understanding of the regional communities from which to recruit subjects, and routinely exceed enrolment and retention targets.
All clinical trials are performed at CCBR’s dedicated Clinical Research Centres. At each Centre, teams of highly trained and experienced clinical staff focus only on clinical research and conducting clinical trials, all of their time. All staff are salaried CCBR employees. CCBR’s strategic network of 16 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 enrolment 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.
We 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.
Every year, our sites undergo 10 to 15 inspections from the FDA, EMEA, local authorities, sponsors, and CROs. We have had no major findings to date. All clinical services are conducted according to ICH-GCP guidelines, applicable CCBR-SYNARC standard operating procedures, and the relevant clinical-study protocol.
At CCBR, we work as partner 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 collaborated 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 more than 20 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
