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ClearTrial Unveils New Product Release at Partnerships in Clinical Trials Conference 2010
Date:4/12/2010

sponsors entering new and emerging countries to conduct trials, ClearTrial v3.2 expands on the software's already extensive, country-specific clinical intelligence. By including labor rates for each country, as well as intelligence around tasks affecting study timelines – such as site activation and regulatory delays – ClearTrial v3.2 makes it easier to model "what-if" scenarios and to generate fast and accurate forecasts of study costs, resource demand, and timelines in any region.

"As our customers’ clinical study processes become more global and more complex, the ClearTrial software continues to lead the market in support of such demands," said Mike Soenen, ClearTrial President and CEO. "ClearTrial v3.2 provides more flexibility in planning and tracking complex global studies while continuing to deliver on our promise to make certain our software is intuitive and easy to use for the wide range of organizations that we serve."

ClearTrial v3.2 New Features Summary

Flexible Enrollment Specification – ClearTrial v3.2 now provides both global and region-specific definition of study enrollment period and distribution. Enrollment distribution has been extended to allow weekly distributions. These new capabilities will enable the user to better accommodate differences in global enrollment performance.

Enhanced Site Approval Forecasting – ClearTrial v3.2 has enhanced its site approval forecasting capabilities to now allow region-specific site approval schedules and the definition of user defined site approval curves. These new features will allow the user to more accurately model site approval schedules.

Advanced Pass Through Costs Definition – ClearTrial v3.2 allows the user greater flexibility in defining pass through and miscellaneous costs. Costs can now be defined at a study or location level, be driven by specific study milestones, and be distributed
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