One Study or a Full Package
Whether you need a single GLP General Toxicology study or a standard core battery of studies for an IND/CTA-enabling package, a dedicated team in Covance’s Greenfield, Indiana facility can provide expertise and scheduling flexibility to meet your preferred timelines.
Get a Comprehensive Program to Support Your IND/CTA-Enabling Package
Emerging biopharmaceutical companies will find our Greenfield, Indiana campus an ideal fit. Onsite drug development leaders have deep expertise in guiding molecules from Lead Optimization through Proof-of-Concept (PoC). We will work with you to provide the optimum level of support and guidance to help you achieve your milestones.
Leverage our Early Phase Development Solutions program and gain a partner who can help you navigate the science, regulatory requirements and complexities of study design required for your program. Working together, we'll help to propel your program forward with continuity, rapid study starts, flexible scheduling and streamlined billing services.
Go Even Further with Specialized Science and Global Expertise
You can conveniently access more of the drug development solutions and scientific experts you need—in Greenfield, Indiana and across the globe. In Greenfield, your continuum of drug development can start at Lead Optimization (Toxicology, Pharmacology), progress through an IND/CTA-enabling program and be supported with our Translational Biomarker Solutions or diagnostic imaging services. Globally, your program is backed by scientific experts and capabilities that you can tap for additional development services; such as immunotoxicology, bioanalysis, or specialized endpoints and routes of administration—to meet your specific molecule requirements.
