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A distinct drug development
experience for your
progressive venture
FOR THE BOLD.
RELENTLESS. YOU.
It’s a program of passion.
Patients are waiting for
a breakthrough. And,
our stakeholders may
only give us one shot.
– biotech client
“
“
You are tenacious.
Determined to navigate the uncertainty and complexity
of today’s drug development requirements.
You pursue the impossible.
Believing new answers are waiting to be unlocked.
You will break through.
With a partner who’s nimble, committed to your pursuit
and has a history of helping biotech firms succeed.
EMBRACE A
UNIQUE APPROACH.
Begin an intimate CRO
partnership with a devoted
team that also offers
exclusive access to the hub
of comprehensive drug
development resources.
WELCOME TO
A TAILORED
EXPERIENCE,
DESIGNED
AROUND YOU.®
Where you get a personalized
engagement from start to finish –
to accelerate your endeavor.
Collaborative Engagement
Looking to stay connected and intimately
involved with the daily operations and
progress of your program? Agile processes,
ongoing communications and innovative
technology make it possible. A devoted
team flexibly adapts to the way you work.
Personalized Attention
Want personalized attention? You got it.
Collaborate with a team devoted to nimble
biopharma programs, who are passionate
about your goals. Plus, gain direct access
to executive advocates to champion your
success and advance your program.
Specialized Expertise
Is stakeholder confidence the ticket to
your success? Don’t compromise. Tap into
specialized expertise – scientific, operational,
regulatory and therapeutic – that puts your
venture on the fast track. Sound advice
and a prospective plan has you navigating
potential pitfalls, insightfully.
More than 1,000
biotech firms choose to
develop their novel drug
with Covance each year.
ENVISION YOUR
SUCCESS.
Gain line of sight to your
entire venture, so you can
easily meet stakeholder
goals and milestones.
Improve your return
 $
600k
each day by streamlining
data delivery for submission
Save up to
30% off
your timelines with a
programmatic approach
Save
~1 year
of patent life on a full
development program
– by reducing time
of ramp-up, data
consolidation and gaps
between phases
•	 Early Phase Development Solutions
•	 Integrated Clinical Pharmacology
•	 Clinical-Biotech
•	 Central Laboratory Services
•	 Biomarkers and Companion Diagnostics
•	 Actionable Data and Analytics
•	 Regulatory and Commercial Consulting
MOVE FROM CANDIDATE
THROUGH COMMERCIALIZATION
•	 Early Phase Development Solutions
•	 MarketPlace
COMPLETE EARLY DEVELOPMENT
AND LICENSE OR SELL ASSET
•	 Integrated Clinical Pharmacology
•	 Clinical-Biotech
•	 Central Laboratory Services
•	 Actionable Data and Analytics
CONDUCT A COMPREHENSIVE
CLINICAL TRIAL
Whichever journey you are on – the hub offers
packages that make sense for your endeavor.
DESIGN YOUR
JOURNEY.
YOUR WAY.
WITH THE HUB.
Regardless of where you are and
how far you aspire to go, you
can advance your program –
comprehensively, economically and
with unprecedented continuity.
With the hub, you have exclusive
access to innovative solutions
designed specifically for nimble
biotech firms. Advance your journey
at your pace, study by study – or
consider an integrated approach with
a combination of complementary
solutions to fit your goals.
MarketPlace
Capitalize on the value of your asset by gaining
critical visibility and establishing the right
connections early with investors and development
partners. Finding your partner may only be a click
away via this unique, online networking solution.
Early Phase Development Solutions
Move swiftly through IND/CTA and into the
clinic 30% faster with a prospective plan and
unprecedented continuity. Your asset is surrounded
with a cross-functional team of experts and proven
efficient processes that save you time and money.
Integrated Clinical Pharmacology
Gain critical data to make earlier and more confident
decisions, by leveraging a global network of clinical
pharmacology units and an integrated approach
to efficiently managed complex trials in healthy
volunteers, patients and special populations.
Clinical-Biotech
Experience a collaborative, flexible approach to your
clinical trial. Engage with an executive lead for the
duration of your program. Gain insights from a devoted
team with scientific, regulatory and therapeutic expertise
in a variety of indications, including oncology and rare
and orphan diseases.
Central Laboratory Services
Enjoy streamlined safety and esoteric testing with
a biotech-dedicated study management team. Get
trial-specific specimen collection kits, unmatched
logistics support and access to scientific expertise.
Biomarkers and Companion Diagnostics
Reach patients who will benefit most from your novel
drug through the power of precision medicine. Go
from pathway selection, biomarker development and
validation to an informed regulatory and commercial
strategy for your companion diagnostic.
Actionable Data and Analytics
Reduce study costs, speed time to market and
increase patient recruitment with visibility into
optimal sites and clusters of eligible participants.
Enable improved enrollment and retention with
proprietary patient diagnostic data, unrivaled site
performance data and unique patient insights.
Regulatory and Commercial Consulting
Advance your nonclinical and clinical strategies,
navigate regulatory requirements and identify the
right approach with a Target Product Profile. Then,
pave the way to commercial success with insights
from early stakeholder and market research.
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.
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
© Copyright 2019 Covance Inc.
BROBPH006-0119
Begin Your Personalized
Drug Development Experience.
Covance.com/TheHub

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