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Whether your firm is large or small and whether you need a stand-alone service or comprehensive support and management of a preclinical study or clinical trial, Covance is ready to serve.

Our broad portfolio of services is designed to help pharmaceutical — and medical device firms — to achieve your drug development goals as efficiently and cost effectively as possible.

To learn how Covance can help you, browse our service areas on the web site:

Some pharmaceutical clients choose to focus their resources on their science. Rather than acquiring specialist regulatory or operations capabilities, they elect to draw on Covance's extensive drug development program management expertise. In this way, they leverage our scientific team's nonclinical, clinical and regulatory experience. We act as project leaders, drawing knowledge from a network of Covance specialists to achieve IND/CTA or NDA goals smoothly and efficiently.
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