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Press Release: iCTRS partners with ViS to revolutionize clinical trial site feasibility assessment

On September 18, 2013, inVentiv Clinical Trial Recruitment Solutions (iCTRS), announced a strategic partnership with ViS Research to revolutionize and speed the antiquated system of clinical trial site evaluation. The partnership with ViS addresses the key problem of clinical trial site evaluation – trial planners simply don’t have adequate analytics about research centers and locations where centers operate. Information is often inaccurate and outdated – or simply does not exist. To find the right trial site, across more than 400,000 research centers worldwide, trial planners send out lengthy feasibility questionnaires, often on paper, that are frequently never filled out or returned. An estimated $10 billion a year is wasted because of poor site selection – the failure to match trial planners with appropriate, effective research sites.

Through its partnership with ViS, iCTRS brings an interactive navigation system to this clinical research universe, so that trial planners can quickly match their needs with the disease-specific capabilities of individual research centers. They can quickly and efficiently evaluate all the relevant analytics – such as local patient population, research activity, infrastructure, personnel, timelines – from the country level through state, city, postal code, all the way down to what is inside the research center facilities.

“We are committed to accelerating clinical research through breakthrough innovation, and this partnership offers trial sponsors the fastest most sophisticated way of ensuring research sites are properly equipped, staffed and ready to be processed for rapid activation,” says Ramita Tandon, senior vice president and general manager for iCTRS. “We are looking forward to building on the remarkable platform and database that ViS already has created.”

Click here for the full press release