Count on timely delivery of accurate release testing results of commercial product or of a development product destined for clinical trials from Covance. Analytical testing issues should not delay product shipping for clinical trials or to patients and when you choose Covance, we ensure you have what you need, when you need it.
As a global leader in GMP-compliant analytical services Covance ensures you have analytical chemists trained and ready for prompt investigation once testing methodology is transferred. A Certificate of Analysis is uploaded to the Covance Study Tracker site (after testing and review are complete) for secure retrieval of your testing results from anywhere in the world.
Flexibility for your schedule
Survey the flexibility with which Covance scientists design, initiate and conduct all aspects of your batch release studies across virtually all dosage forms and delivery technologies.
Make Covance your partner of choice
Expand your resources with the instrumentation and infrastructure capacity Covance maintains and rest assured that with our strong regulatory inspection history, there are no unpleasant surprises awaiting you.
Access to cGMP analysis of radiolabeled dose for human AME (absorption, metabolism and excretion) studies is yours with our nuclear license and other unique advantages and experience. To learn more, click here to download our service profile.