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Graphically height-ed claim: 48/50 of the best selling drugs of 2013 were developed with Covance Central
Your ideas make it possible. Our solutions make it happen.
THE POWER OF NEW POSSIBILITIES.What happens when the largest, most trusted central laboratory and the broadest array of specialty clinical testing services come together?
Reveal new opportunities and insights by partnering with our team of dedicated scientists and operational experts.
Covance accelerates your clinical testing through unique insights, globally consistent processes and a commitment to on-time data delivery.
Something new.Something powerful.Something unique.
48 OF THE 50BEST-SELLINGDRUGS OF 2015WERE DEVELOPEDIN PARTNERSHIPWITH COVANCE
We generate more clinical trial data than
any other central laboratory in the world.
YOUR PROTOCOL WILL BE THE STARTING POINTIt will be at the center of everything we do
• We will bring the unique insight that only the most experienced lab can provide.
• Complex biomarkers? Remote sites? No problem. We have solutions for that.
• Working together, we will conduct an efficient study, yielding more statistically powerful data.
WE UNDERSTAND YOUR SCIENCEWe put practically any test at your fingertips. Effortlessly.
5,100+STUDIES
IN THE LAST 5 YEARS
You get the insight you need to make better decisions. Sooner.
YOUR TIMEIS MONEY.Our experience
delivers results.
Faster.
• Diverse assay development platforms
that reveal elusive biomarker solutions
in the discovery/exploratory phase.
600+ASSAYSARE DONE WITHIN
OUR CENTRAL LABS
3,000+ASSAYSAND THE SCIENTISTS THAT
VALIDATED THEM — ARE
AVAILABLE WITHIN OUR LABCORP
SPECIALITY TESTING GROUP AND
MANAGED ACCORDING TO CLINICAL
TRIAL STANDARDS, FROM A TOTAL
MENU OF OVER 4,500 ASSAYS.
• Proven solutions for CDx and personalized
medicine that give you a new perspective
on your path to commercialization.
Whether you are pursuing an in vitro diagnostic (IVD) or a lab developed test (LDT) that can be FDA-approved as a companion diagnostic, we are ready to support your personalized medicine program. Each of these pathways requires highly specialized technical, regulatory and commercial insight.
CDx DEVELOPMENTMore proven pathways to success
In 2015 alone, we worked on
60+ CDx PROGRAMSsupporting more than
125 CLINICAL PROTOCOLSin most therapeutic areas such as cardiovascular, CNS, infectious disease, inflammation and oncology.
We provide expertise in:
Regulatory submissionCommercialization
Development
Market access
Validation
Testing
21
345
6
We have helped bring MORE THAN 80 APPROVED DIAGNOSTIC TESTS to market through collaborations with diagnostic test developers.
Together, Covance and LabCorp have the proven experience required
TO SUCCESSFULLY DEVELOPAND COMMERCIALIZE YOURNEXT COMPANION DIAGNOSTIC.
EXECUTE YOUR CLINICAL TRIALS WITH CONFIDENCEGlobally consistent platforms ensure data quality
REVEAL NEWCOMMERCIALIZATIONOPPORTUNITIESExceptional statistical power lets you
uncover even the smallest differences in
physiological response to drug candidates.
EVERY PATIENT COUNTSAutomation from kit
production through data
delivery speeds results,
improves consistency
and reduces test
cancellations.
*data source: Life Science Strategy Group Survey, 2016
Dependable, proactive logistics
process and experienced
contingency planning deliver
>99% SAMPLERECEIPT WITHINSTABILITY.
EXPANDED LABORATORY MANAGEMENT SOLUTIONSEnsure testing performed outside
the central lab is backed by rigorous
quality agreements.
We were the first central lab to meet
ISO 15189:2012STANDARDS.
ENROLL FASTERInvestigator sites prefer Covance Central Laboratory Services*
INVESTIGATOR SITES PREFER COVANCECENTRAL LABORATORY SERVICES3X
BRING THE POWER OF SCALE TO YOUR TRIAL, NO MATTER HOW LARGE… OR SMALL
4.6 MILLION+CUSTOM KITSper year
99.993%ACCURACY
97.7%ON TIME FIRST SUPPLIES
25,000KIT CAPACITYper day
GLOBAL AUTOMATED KIT PRODUCTION FACILITY
SAMPLE RECEIPT WITHIN STABILITY
Investigator training & global logistics drive:
BETTER DECISIONS, FASTER
CONSISTENT SAMPLE COLLECTION AND PROACTIVE LOGISTICS
PRE-ANALYTICAL AUTOMATIONSaves time...saves money...saves samples
• Efficient barcode scanning
• Missing samples identified within 1 minute
• 80% container re-use saves money...and our environment
You may have a Phase III study needing thousands of sites. Or a small trial, with just a single Phase I clinic. Or a specialty biomarker validation. Whatever the scale of your trial, experience precision delivery based on thousands of trials across all therapeutic areas.
LABLINK+ ONLINE DATA ACCESS• Results available within minutes for fast access
• Customizable reports
99.2%
HEMATOLOGY AUTOMATION• Hardware and software automation
• Results hours earlier
• Consistency you can trust
YOUR UNIQUE TRIAL. OUR DIVERSE CAPABILITIES.CUSTOMIZED SOLUTIONS.
DIVERSE GLOBALLABORATORY SOLUTIONSStarting with your protocol, we will develop
a customized solution drawing from our
unmatched suite of testing capabilities.
Don’t get boxed in by a niche lab with limited capabilities.
AN AGILE PARTNERFOCUSED ON YOUR SUCCESS
Trialneeds
Central labs
Phase I solutions
Genomics solutions
Covance bioanalytical services
Translational biomarker solutions
LabCorp Specialty Testing Group
External labs
LET’S BEGIN THE CONVERSATIONabout how we can work together to transform your clinical trial with our testing solutions.
Covance Inc., headquartered in Princeton, NJ, USA, is the drug development business of
Laboratory Corporation of America Holdings (LabCorp). COVANCE is a registered
trademark and the marketing name for Covance Inc. and its subsidiaries around the world.
© Copyright 2016 Covance Inc. BROCLS031-1116
The Americas +1.888.COVANCE (+1.888.268.2623) +1.609.452.4440
Europe / Africa +00.800.2682.2682 +44.1423.500888
Asia Pacific +800.6568.3000 +65.6.5686588
Visit:www.covance.com/clsfor more information.
REMEMBER:TIME IS MONEY. SO DON’T WAIT.
WE THINK OUTSIDE OF THE BOX TO GIVE YOU THE MOST TESTING OPTIONS.