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Saturday, September 12, 2015 1:24:56 PM
Pre-Study
The imaging Endpoints team, comprised of some of the most experienced industry experts and former FDA leaders, identifies the best imaging for your trial, assists in protocol development, generates all study documentation and standardizes image acquisition across all clinical sites. We specialize in setting up all required systems and procedures to enable real-time image QC, query resolution, reads and reporting. We emphasize training and establish metrics that ensure your performance requirements are constantly measured, reported and met or exceeded.
During Study Conduct
Imaging Endpoints collects images real-time from sites globally and our radiology technologist perform image QC and query resolution until the query is resolved. We track and report clinical site performance metrics real-time and quickly retrain clinical site staff to minimize protocol variances.
Through an imaging clinical trial management system (iCTMS), state-of-the-art analysis software, in-house radiologists and expert data management, we provide real-time reads and rapidly report the results to you. We leverage our easily customizable iCTMS and superior project management to report monthly progress metrics that meet your exact requirements.
Post-Study
At the end of your trial, Imaging Endpoints provides secure transmission of all image data in the format you require. Included are data clean/lock, long-term data storage (with on-site and off-site daily backup) as well as transfer of all images with viewing software. We write the imaging components of regulatory submissions, and our medical, scientific and statistical experts generate the most advanced imaging analysis reports in the industry.
http://www.imagingendpoints.com/about/what-we-do
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