YPrime’s IRT+ goes beyond traditional IRT capabilities of patient randomization and drug supply management with control and a real-time view into critical functions and flows of a clinical trial - involving patient interactions, site activities and clinical supply management.
Customizable and configurable functionality is built directly to specifications in an agile, iterative development process that compresses traditional timelines. Through system design recommendations and ongoing support throughout your clinical trial. YPrime’s experienced IRT project managers can help avoid known pitfalls and scenarios with potential unintended consequences. Our project managers are trained in best practices to communicate risk, report on timelines, and manage scope.
IRT+ is a uniquely powerful tool to simplify clinical trial management:
During system development, clients are involved every step of the way, resulting in an efficient delivery with no surprises at the user acceptance testing stage. IRT+ provides the precision needed to advance to the next development milestone.
Flexibility and Speed
YPrime’s standards are exacting and stringent. Our teams follow clearly documented quality control procedures to ensure consistent and accurate results. We retain experienced staff who are accessible and ready to help throughout the implementation and maintenance of all projects.