Program Management
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IND/CTA-enabling Services
A well-designed development strategy is crucial to the success of a drug candidate. As new drugs proceed into clinical development, Covance's Program Management team works with you to develop a cost-efficient strategy to address key safety and regulatory issues, and enable clinical testing in human volunteers.
The Covance Program Managers are pharmaceutical scientists who average 20 years of experience in drug development, and are available to help you customize your drug development strategy. Program Managers integrate the complete array of Covance services, including safety pharmacology, toxicology, pathology, drug metabolism and pharmacokinetics to assure successful design and conduct of your program.
IND/CTA-Enabling Services
- Genetic and Molecular Toxicology
- Mammalian Toxicology
- Safety Pharmacology
- Bioanalytical
- Drug Metabolism
- Dose Formulations
- Program Management
- StudyTracker®
- Regulatory
- Pre-IND meetings
- Investigator's Brochure
- IND/CTA preparation
- GMP Analytical Support
- Pharmacokinetics.
Nonclinical Resources
- Worldwide Senior Scientific Staff
- Toxicology: 128
- Pathology: 33
- Drug Metabolism: 53
- Bioanalytical: 56
- Analytical and Stability Services: 23
- Program Management: 15
- Facility Locations
- North America
- Madison, WI
- Vienna, VA
- Indianapolis, IN
- Chantilly, VA
- Europe
- Harrogate, UK
- Münster, Germany.
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