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Discover how our expanded capabilities in GLP Toxicology at our Greenfield, Indiana campus can make a difference for your clients next IND/CTA-enabling program.
With your clients’ increased demand for toxicology services, they rely on your expertise to help them find comprehensive and consistent support for GLP and non-GLP toxicology studies.
Now, you can access expanded GLP safety assessment at our Greenfield, Indiana campus to meet both standard and specialized needs – providing you five GLP toxicology-enabled sites globally: Madison, WI (U.S.); Harrogate, UK; Münster, Germany; Shanghai, China; and now Greenfield, IN (U.S.).
Finding the best fit for your client
Supporting IND/CTA-enabling packages
An optimal level of support and guidance is critical for meeting early drug development milestones. To support your client’s goals, you'll find:
Standard core-battery studies: Starting with Lead Optimization with toxicology and pharmacology, your client can tap into our non-GLP or GLP capabilities.
Comprehensive support: With support from our Early Phase Development Solutions program, your client can leverage our global experience to navigate the science, regulatory requirements and complexities of study design.
Convenient access: From supporting immunotoxicology, bioanalysis, translational biomarkers and even working with specialized endpoints and routes of administration, we can easily handle unique requirements.
Flexibility: Expect our dedicated teams to meet your client’s schedule with rapid study starts, flexible scheduling, quick-turn results and streamlined billing services.
Consistency counts. Now with expanded support for GLP General Toxicology, your client has more options in their drug development journey.
Ensure your clients can achieve their study goals.