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goBalto Sponsors Tufts CSDD Study to Benchmark the Clinical Trial Initiation Process
Date:11/17/2011

SAN FRANCISCO, November 17, 2011 /PRNewswire/ --

goBalto, developer of new generation web-based clinical research solutions, announced that it is providing a research grant for the Tufts Center for the Study of Drug Development (Tufts CSDD) to benchmark the clinical trial initiation process.  Currently there is virtually no industry data available on the typical process that companies follow and on the amount of time that this process takes.

Tufts CSDD, an independent, non-profit academic research group at Tufts University in Boston, routinely conducts benchmark studies of critical drug development functions and activities.  For this study, fifteen international biotechnology and pharmaceutical companies and clinical research organizations (CROs) will provide data on their experience initiating clinical trials.  Tufts CSDD will discuss the study aims and methodology at Informa's site feasibility and study start-up conference in London on December 6-7, 2011.

"This study will map the steps and duration of the clinical trial initiation process," said Ken Getz, senior research fellow at Tufts CSDD and principal investigator on the project. "We anticipate identifying critical insights that sponsors and CROs can use to accelerate their study start-up times and drive higher levels of efficiency and effectiveness in the process."

goBalto also announced a strategic partnership with Genexion, a full-service CRO that has selected Tracker™, goBalto's web-based clinical trials platform, for its clinical research study start-up and monitoring.

"We're delighted to be collaborating with the Tufts Center to study this important topic and look forward to the learnings that the industry will draw from the study findings," said Jae Chung, founder
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SOURCE goBalto
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