You gain instant expertise from your global Covance infrastructure of data experts whose only job is to support you through the rigors of global or local drug development, from phase I through phase IV clinical trials. Our teams are comprised of:
- Data managers
- Case report form (CRF) designers
- SAS® programmers
- Medical writers
- Project Management
Our global Clinical Data Analysis and Reporting organization is a centralized team that shares and provides operational excellence by delivering timely, accurate clinical trial data (packaged or as individual services), enabling you to make faster and more effective decisions about the safety, tolerability and pharmacokinetic /pharmacodynamic properties of your compound.
Centers of Excellence
Covance phase I/II activities are centralized into two centers of excellence, with teams based in Madison, Wisconsin (USA) and Leeds, England. We offer data analysis and reporting services as a comprehensive package or individually.