Analysis Shows Feasibility Studies Could be Conducted in Half the Time

Jan 23, 2014
By Applied Clinical Trials Editors

Last September, inVentiv Clinical Trial Recruitment Solutions (iCTRS), announced its strategic partnership with ViS Research to address the challenges of clinical trial site evaluation. Four months later, the company has released analysis that could prove potential savings in the ViS platform for clinical trial feasibility studies. iCTRS took data from 100 feasibility studies conducted by inVentiv and analyzed the time required to perform each of the individual tasks involved in such studies. iCTRS then looked at how much time the application of ViS technology could save for each task. Cumulatively, the efficiencies offered by ViS cut the total feasibility study hours by 54% -- while delivering better quality.

Read the full release here.

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