Registries and observational studies are vital instruments to understand and improve health care over time. Draw upon Covance's accumulated global expertise since 1997 for streamlined clinical trials across an array of products, therapeutic areas and disease states.

Take the Covance Approach

• Limit study burden to allow full visibility for registry conduct
• Begin with simplified design protocols rooted in sound epidemiological rigor
• Develop and implement streamlined protocols and recruitment documentation
• Maximize use of central IRBs
• Create user-friendly materials for study sites and patients
• Follow clinical practice operations under real world conditions
• Provide highly configurable data acquisition solutions for rapid reporting of study results

Effective Tools for Registries and Observational Studies

• Covance observational study & registry application (COR)- a web-based proprietary data collection tool
• Data collection instruments that target well-defined endpoints
• Focused-response electronic case report forms (eCRFs) to ensure accurate data capture
• Efficient and cost-effective options tailored to your specific situation for rapid data capture, tracking, reviewing and processing
• Strategic information extraction from registries and observational studies to improve the quality of health care

Your Success Is Part of Our Grand Design

• Covance Periapproval Services believes that a successful registry begins with its design.
• Our simplified design protocols are rooted in sound epidemiological rigor and follow clinical practice operations under real world conditions to ensure your trial is designed in a way that is practical when implemented in actual clinical practice.