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Covance, with headquarters in Princeton, New Jersey, is one of the world’s largest and most comprehensive drug development services companies, with annual revenues greater than $2 billion, employees in more than 60 countries, and more than 15,000 employees worldwide. NONCLINICAL DEVELOPMENT (Toxicology, Research Products, Analytical Services) Covance Early Development supported 82% of the drugs approved by the FDA in 2016: - 13 global facilities with 3,800+ staff - 600+ clients served per year - ~12,000 studies conducted per year - 300+ IND-CTA-enabling programs delivered in past 5 years CLINICAL DEVELOPMENT (Clinical Pharmacology, Clinical, Central Labs) -Supported 50% of latest breakthrough cancer treatments -Supported development of the top 25 currently marketed medicines -70% of clinical programs on or ahead of enrollment timelines -Broad-based, scalable and market-leading, -Biomarker capability ->99% of samples received within stability In the last 5 years (2011-2015), we participated in >4400 studies, >240M tests, >90 countries, >1.3M patients, >140k patients. Note, these are all Covance only; LCT numbers not yet folded in, so eventual numbers will be higher when final 2012-2016 numbers are posted in a month or two. -Five Clinical Pharmacology units with over 350 beds PERIAPPROVAL & MARKET ACCESS -Results-driven reimbursement support for >60% of the biologics market -Designed and managed world’s largest safety registry ever – iPledge -Team of experts dedicated to risk management and Pharmacovigilance -Bi-coastal call center capabilities to deliver patient and physician support
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