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endpoint Saves Money and Time for Medical Research Teams Through PULSE
Date:2/9/2010

SAN FRANCISCO, Feb. 9 /PRNewswire/ -- endpoint Clinical (www.endpointclinical.com), a leader in Integrated Voice Response (IVR)/Integrated Web Response (IWR) systems, announced today that PULSE, a fully configurable platform that allows users to design and deploy clinical trial Integrated Response Technology (IRT) systems, saves 40 percent on the development time of clinical trials. This time and cost savings stems from PULSE's ability to provide pre-validated programs so developers do not have to spend valuable time re-configuring studies. For some studies, endpoint will deliver a validated study program in just four weeks rather than eight weeks.

endpoint's PULSE engine gives more control to Clinical Program Managers by allowing them to perform mid-study changes on the fly. Because endpoint's platform contains pre-validated programs, clinical trials can move ahead at a more rapid rate due to project managers having access to the configurable design elements available by PULSE rather than relying on custom development for each change.

"PULSE literally puts the power in the hands of the program manager rather than going through the development team which consumes more time," said Jonathan Dole, co-founder and CEO, endpoint. "Shaving weeks off of the development process for the clinical trial process, PULSE is the holy grail for pharmaceutical and medical companies who want to streamlin
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