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Only Covance combines one of the world’s largest sources of de-identified lab results and patient intelligence data with investigator data from the majority of global clinical trials that provide insights to increase efficiencies and effectiveness in clinical drug development.
Find patients that Meet Your Inclusion/Exclusion Criteria
Using LabCorp’s real world, de-identified clinical laboratory data on over 150 million patients, we can assess populations who meet your protocol’s eligibility criteria, accurately model the impact that the protocol inclusion/exclusion criteria will have on the patient pool size and geo-locate
Pinpoint Investigators
Covance generates more clinical trial data than anyone else in the world. Our global proprietary data helps us predict future investigator performance and capacity to run multiple studies.
Strengthen Your Protocol with Patient Insights
Design your protocol around actual feedback from potential patients to elevate your recruitment and retention rates.
Combining four unique data sets with our therapeutic and functional expertise, Covance can impact protocol design and feasibility, optimal site selection, and patient recruitment.
*Savings based on an analysis of trials processed through Covance Central Labs with Protocol Finalization date after 1/1/2009 for the specific clinical indications. Past performance is not a guarantee of future results, and a variety of factors other than CRO performance can impact timing of clinical studies.