Return-On-Investment

Once internal business processes and stakeholders needs have been defined and captured as standard IRT requirements, our flexible system can build off of this study template to provide efficient, consistent system builds for similar future studies.  This use of the template adds a percentage of savings which is expected or has been seen in other opportunities in which the tactic was implemented.

IRT Custom Xpress uniquely maximizes return-on-investment by reducing timelines, and yielding significant efficiencies in the following areas:

• IRT Custom Xpress increases study accuracy and efficiency
• IRT Custom Xpress implementations are dramatically accelerated from the 8-12 week industry standard to just 4-5 weeks 
• Overall study cost reduction via IRT integration with Electronic Data Capture, Clinical Trial Management, and Drug Supply Inventory Management Systems, and Electronic Patient Reported Outcomes of  invivodata EPXTM ePro
• Enhances custom reporting and analytics capabilities powered by SAP BusinessObjects