Throughout the drug development cycle, regulatory approvals are highly dependent on the laboratory data that is generated in clinical trials. The unbiased data that a central laboratory provides is of critical importance in any clinical trial.
At Eurofins Central Laboratory, we fully understand the necessity and importance of harmonizing our laboratory operations to ensure that the laboratory testing results generated in any one of our global facilities can be easily combined. Utilization of global standard operating procedures, uniform instruments, reagents and analytical methods for safety testing enables the use of universal reference ranges, resulting in accurate laboratory data that are completely combinable.