CCBR has a unique capability in the performance of clinical research. Our global coverage of dedicated CCBR trial centres has greater access to patients, better training and expertise in GCP, more resources and equipment and higher quality processes than most ordinary centres taking part in clinical trials. All CCBR centres are trained to same high level and are following the same Standard Operating Procedures.
Therapeutic Area Knowledge
CCBR provides professional input to the development of clinical protocols where we align the FDA guidance for industry with the Sponsors requirements to differentiate from competitors. Our background in science and opinion leading insight enables us to contribute to the successful conduct of clinical programmes.
Investigator Site Capacity
CCBR sites are located, resourced and equipped for the enrolment and treatment of large numbers of patients taking part in clinical research.
CCBR consistently contributes with high performing sites in clinical trials. We develop study specific strategies for patient recruitment, including direct contact with potential participants through our established database, which ensures that we can meet or exceed our enrolment targets.
From screening to randomization, visit management and follow up, CCBR conducts all the clinical procedures required by the protocol. Our standards of patient care ensure that patient retention rates are consistently high. In addition, our proven performance in delivery of and compliance with the protocol results in quality and consistency of data that is unmatched.