Are you interested in faster clinical trials and improved data quality? For most sponsors and CROs, the answer would be an emphatic "Yes!" Managing a clinical trial effectively requires collaboration across multiple trial requirements. This presentation illustrates how IVR/IWR and lab data can be integrated and reconciled in real-time, improving the speed and overall quality of trial results. This presentation uses real-life case studies to demonstrate the trial efficiencies and benefits gained when combining labs and IVR/IWR data in real-time. The speaker also discusses technical considerations to enable an integrated data stream.

This audio conference covers:

• Techniques for integrating lab and IVR/IWR data
• Trial benefits that can be realized by integrating data streams
• How to utilize lab results for randomization and the benefits of doing so
• A real-life case study on optimizing the management of lab kits and ancillary supplies
• Benefits of using IVRS to track lab samples

About the speaker:

Vicky Czarnik is a Senior Technical Strategy Manager with Covance's Interactive Voice Response Services. In this role she helps sponsors develop interactive voice response system (IVRS) strategies, identify ways they can leverage IVRS solutions to increase efficiencies, identify synergies across clinical functions, gain cost savings, and improve productivity. Vicky has been intimately involved with the implementation of some of Covance’s latest service offerings, including the IVRS Express Suite and their latest technology solution, the interactive web response system (IWRS). Since joining Covance in 2000, she has worked on over 40 clinical trials, spanning a variety of therapeutic areas including allergy, cardiovascular (including critical care), dermatology, diabetes/endocrinology, gastroenterology, hematology, infectious diseases, musculoskeletal, neurology, oncology and respiratory, with over 20 pharma/biotech companies and over 15 CRO, drug packaging/distribution, and EDC vendors.

Who should attend?

• Clinical Logistics Managers
• Drug Supply Managers
• Clinical Operations Managers
• Clinical Supply Chain Coordinators
• Outsourcing Managers
• Project Managers (clinical, IVRS, central labs)
• Clinical Trial Managers
• Study Team Leaders
• Site Managers

*This conference is rated General interest.