Xcellerate® Clinical Trial Optimization®
Research shows that clinical trial enrollment comes up short a good 50% of the time, which costs you valuable time and money. But now there’s a unique new way to better predict which clinical sites are likely to deliver the right patients. So you can engage them from the start and avoid sites that are more likely to underperform.
Xcellerate, helps ensure more cost-effective and timely clinical trials. Providing cutting edge site and investigator selection tools, clinical trial scenario planning, forecasting and resource management, Xcellerate can help you achieve a better return on your clinical investment.
Xcellerate is the only data-driven drug development approach that harnesses the power of the largest clinical trial knowledgebase in the industry. Our knowledgebase incorporates data from clinical trials including over 7,000 completed protocols covering 500 indications and 125,000 unique investigators who have had over 10 million patient visits. We analyze this data, together with information from large, public data sources including the FDA 1572 data, clinical trials.gov and other purchased data sets with a unique approach to provide you with study-specific recommendations.
Xcellerate is part of every trial we manage and will enable you to benefit from
- The industry’s largest clinical trial knowledgebase
- Enhanced site selection and performance prediction
- Scenario modeling tools
- Improved prediction of site activation sequencing
- Superior trend analysis
On Demand Webinars
Clinical Trial Optimization
Improving Return on Clinical Investment
by Susan Schenk
Director, Operational Strategy & Planning
This recent Webinar invites you to find out more about a new way to better predict which clinical sites are most likely to deliver the right patients. So you can engage these sites from the start and avoid sites that are more likely to under-perform.
In the Webinar, Susan Schenk, Director of Operational Strategy & Planning at Covance, explores new approaches to Clinical Trial Optimization™ to help enable more cost-effective and timely clinical trials. The Webinar discusses pragmatic approaches and real-life case studies as well.
3 good reasons to view the Webinar recording
- Ensure studies are designed and executed with quality built in and the best chance of enrollment success
- Identify the investigators most likely to meet performance expectations
- Build more reliable benchmarks for predicting possible future site enrollment performance
Optimizing Clinical Trial Performance:
A Partnership Planning & Management Approach
by Paul R. Bunch, Ph.D., PMP
Vice President & Head, Global Project Management, Clinical Development Services
Measuring the success of a sponsor-CRO partnership can be challenging for a number of reasons including differences in perspective and the need to measure a broad variety of success factors.
This Webinar reviews a partnership approach that has been successfully implemented to plan, monitor, and control the performance of both individual clinical trials and a portfolio of clinical trials. A case study on earned value metrics takes a central place to illustrate how sponsors and Covance have developed innovative measures and improvement strategies to ensure the collaboration success.
The second in a series of Webinars exploring new approaches to Clinical Trial Optimization™, in this interactive Webinar,
Paul Bunch, Vice President & Head of Global Project Management at Covance, shares his extensive firsthand experience and focuses on practical approaches and tools. Real life examples will be included, and your questions and comments are warmly welcomed.
3 good reasons to join the Webinar
- Find out more about metrics used to assess performance trends and identify areas for improvement
- Explore a management process that integrates with the measurement system to drive performance improvement
- Discuss how the process and metrics can be used to improve the accuracy of planning processes