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Global Coverage - Standardization

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Global standardization

Throughout the drug development cycle, regulatory approvals are highly dependent on laboratory data generated in clinical trials. The unbiased data that a central laboratory provides is of pivotal 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 results generated in our facilities around the world can be easily combined. Utilization of global standard operating procedures, uniform instruments, reagents and analytical methods for safety testing enable the use of global reference ranges, resulting in global laboratory data that are truly combinable.

For further information please contact: clinicaltrials@eurofins.com